A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655379



Internal ID15392031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110836356..110843727hg38UCSC Ensembl
Innerchr1:111378978..111386349hg19UCSC Ensembl
Innerchr1:111180501..111187872hg18UCSC Ensembl
Innerchr1:111091020..111098391hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg387372
hg197372
hg187372
hg177372
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv655379
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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