A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657243



Internal ID15047209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3760396..3773958hg38UCSC Ensembl
Innerchr4:3762123..3775685hg19UCSC Ensembl
Innerchr4:3731921..3745483hg18UCSC Ensembl
Innerchr4:3799092..3812654hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3813563
hg1913563
hg1813563
hg1713563
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519631
Supporting Variants
Samples
Known GenesADRA2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657243
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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