A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683456



Internal ID15420108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11312581..11338308hg38UCSC Ensembl
Innerchr1:11372638..11398365hg19UCSC Ensembl
Innerchr1:11295225..11320952hg18UCSC Ensembl
Innerchr1:11306904..11332631hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3825728
hg1925728
hg1825728
hg1725728
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516050
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683456
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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