A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv436937



Internal ID15383178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39709808..39711514hg38UCSC Ensembl
Outerchr4:39692694..39736585hg38UCSC Ensembl
Innerchr4:39711428..39713134hg19UCSC Ensembl
Outerchr4:39694314..39738205hg19UCSC Ensembl
Innerchr4:39387823..39389529hg18UCSC Ensembl
Outerchr4:39370709..39414600hg18UCSC Ensembl
Innerchr4:39608608..39610314hg16UCSC Ensembl
Outerchr4:39591494..39635385hg16UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3843892
hg1943892
hg1843892
hg1643892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv466818
SamplesNA12707
Known GenesUBE2K
MethodSNP array
AnalysisOur algorithm aims to detect deletions that are transmitted from a hemizygous parent to a child. For each trio, every SNP was coded into one of seven categories: (A) Type I mendelian incompatibility (that is, consistent with deletion) involving mother; (B) Type I mendelian incompatibility involving father; (C) Type II mendelian incompatibility (that is, inconsistent with deletion); (D) child homozygous or missing data, both parents homozygous or missing data; (E) child homozygous or missing data, father heterozygous, mother homozygous or missing data; (F) child homozygous or missing data, mother heterozygous, father homozygous or missing data; (G) child heterozygous or both parents heterozygous (see Supplementary Methods for further details). SNPs were assigned to states D-G only if they did not contain mendelian incompatibilities. A run of consecutive SNPs in a particular trio was considered to be consistent with a maternal transmitted deletion if all SNPs were in states A, D or E, or with a paternal deletion if all SNPs were in states B, D or F.
PlatformNot reported
Comments
ReferenceConrad_et_al_2006
Pubmed ID16327808
Accession Number(s)nsv436937
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer