A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702605



Internal ID15092571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10488368..10493538hg38UCSC Ensembl
Innerchr6:10488601..10493771hg19UCSC Ensembl
Innerchr6:10596587..10601757hg18UCSC Ensembl
Innerchr6:10596587..10601757hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg385171
hg195171
hg185171
hg175171
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520598
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702605
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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