A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697276



Internal ID15087242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:202008699..202009195hg38UCSC Ensembl
Innerchr1:201977827..201978323hg19UCSC Ensembl
Innerchr1:200244450..200244946hg18UCSC Ensembl
Innerchr1:198709484..198709980hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38497
hg19497
hg18497
hg17497
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516812
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697276
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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