A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660346



Internal ID15396998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:79854802..79856517hg38UCSC Ensembl
Innerchr6:80564519..80566234hg19UCSC Ensembl
Innerchr6:80621238..80622953hg18UCSC Ensembl
Innerchr6:80621238..80622953hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg381716
hg191716
hg181716
hg171716
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516620
Supporting Variants
Samples
Known GenesC6orf7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660346
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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