A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677582



Internal ID15414234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100432820..100462922hg38UCSC Ensembl
Innerchr6:100880696..100910798hg19UCSC Ensembl
Innerchr6:100987417..101017519hg18UCSC Ensembl
Innerchr6:100987417..101017519hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3830103
hg1930103
hg1830103
hg1730103
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515895
Supporting Variants
Samples
Known GenesSIM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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