A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437367



Internal ID15382673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28943586..28947128hg38UCSC Ensembl
Outerchr4:28938521..28961306hg38UCSC Ensembl
Innerchr4:28945208..28948750hg19UCSC Ensembl
Outerchr4:28940143..28962928hg19UCSC Ensembl
Innerchr4:28554306..28557848hg18UCSC Ensembl
Outerchr4:28549241..28572026hg18UCSC Ensembl
Innerchr4:28696091..28699633hg16UCSC Ensembl
Outerchr4:28691026..28713811hg16UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3822786
hg1922786
hg1822786
hg1622786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv467248
SamplesNA19240
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)nsv437367
Frequency
Sample Size60
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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