A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705128



Internal ID15095094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99336998..99353592hg38UCSC Ensembl
Innerchr4:100258155..100274749hg19UCSC Ensembl
Innerchr4:100477178..100493772hg18UCSC Ensembl
Innerchr4:100615333..100631927hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3816595
hg1916595
hg1816595
hg1716595
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528518
Supporting Variants
Samples
Known GenesADH1C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705128
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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