A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698637



Internal ID15088603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:112841393..112858368hg38UCSC Ensembl
Innerchr1:113384015..113400990hg19UCSC Ensembl
Innerchr1:113185538..113202513hg18UCSC Ensembl
Innerchr1:113096057..113113032hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3816976
hg1916976
hg1816976
hg1716976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522967
Supporting Variants
Samples
Known GenesLOC100996702
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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