A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695291



Internal ID15431943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:235887907..235890872hg38UCSC Ensembl
Innerchr1:236051207..236054172hg19UCSC Ensembl
Innerchr1:234117830..234120795hg18UCSC Ensembl
Innerchr1:232377248..232380213hg17UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg382966
hg192966
hg182966
hg172966
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517883
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695291
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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