A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697094



Internal ID15087060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155676929..155690151hg38UCSC Ensembl
Innerchr4:156598081..156611303hg19UCSC Ensembl
Innerchr4:156817531..156830753hg18UCSC Ensembl
Innerchr4:156955686..156968908hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3813223
hg1913223
hg1813223
hg1713223
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519870
Supporting Variants
Samples
Known GenesGUCY1A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697094
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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