A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703766



Internal ID15093732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42122345..42163782hg38UCSC Ensembl
Innerchr4:42124362..42165799hg19UCSC Ensembl
Innerchr4:41819119..41860556hg18UCSC Ensembl
Innerchr4:41965290..42006727hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3841438
hg1941438
hg1841438
hg1741438
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527340
Supporting Variants
Samples
Known GenesBEND4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703766
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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