A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516620



Internal ID15443913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:79854802..79863565hg38UCSC Ensembl
Innerchr6:80564519..80573282hg19UCSC Ensembl
Innerchr6:80621238..80630001hg18UCSC Ensembl
Innerchr6:80621238..80630001hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg388764
hg198764
hg188764
hg178764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660346, nssv673859, nssv669608, nssv674011, nssv677201, nssv685186, nssv682991, nssv682188
Samples
Known GenesC6orf7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516620
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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