A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658960



Internal ID15395612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110798535..110843727hg38UCSC Ensembl
Innerchr1:111341157..111386349hg19UCSC Ensembl
Innerchr1:111142680..111187872hg18UCSC Ensembl
Innerchr1:111053199..111098391hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3845193
hg1945193
hg1845193
hg1745193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517082
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658960
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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