A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700445



Internal ID15437097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100446711..100462922hg38UCSC Ensembl
Innerchr6:100894587..100910798hg19UCSC Ensembl
Innerchr6:101001308..101017519hg18UCSC Ensembl
Innerchr6:101001308..101017519hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3816212
hg1916212
hg1816212
hg1716212
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)nssv700445
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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