A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698147



Internal ID15434799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:49169327..49201701hg38UCSC Ensembl
Innerchr6:49136963..49169337hg19UCSC Ensembl
Innerchr6:49244922..49277296hg18UCSC Ensembl
Innerchr6:49244922..49277296hg17UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3832375
hg1932375
hg1832375
hg1732375
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521530
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698147
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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