A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437382



Internal ID15382688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64644772..64648006hg38UCSC Ensembl
Outerchr4:64638996..64648376hg38UCSC Ensembl
Innerchr4:65510490..65513724hg19UCSC Ensembl
Outerchr4:65504714..65514094hg19UCSC Ensembl
Innerchr4:65193085..65196319hg18UCSC Ensembl
Outerchr4:65187309..65196689hg18UCSC Ensembl
Innerchr4:65513870..65517104hg16UCSC Ensembl
Outerchr4:65508094..65517474hg16UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg389381
hg199381
hg189381
hg169381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467263
SamplesNA19208
Known Genes
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)nsv437382
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