A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515895



Internal ID15442952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100420903..100462922hg38UCSC Ensembl
Innerchr6:100868779..100910798hg19UCSC Ensembl
Innerchr6:100975500..101017519hg18UCSC Ensembl
Innerchr6:100975500..101017519hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3842020
hg1942020
hg1842020
hg1742020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672248, nssv677741, nssv674785, nssv692812, nssv688559, nssv692010, nssv677582, nssv671135, nssv667008, nssv687417, nssv684841, nssv673721, nssv674756, nssv665180, nssv683246, nssv700445, nssv657822
Samples
Known GenesSIM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515895
Frequency
Sample Size2026
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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