A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700091



Internal ID15090057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163498485..163517299hg38UCSC Ensembl
Innerchr6:163919517..163938331hg19UCSC Ensembl
Innerchr6:163839507..163858321hg18UCSC Ensembl
Innerchr6:163889928..163908742hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3818815
hg1918815
hg1818815
hg1718815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524205
Supporting Variants
Samples
Known GenesQKI
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700091
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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