A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516840



Internal ID15444133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139639696..139732567hg38UCSC Ensembl
Innerchr6:139960833..140053704hg19UCSC Ensembl
Innerchr6:140002526..140095397hg18UCSC Ensembl
Innerchr6:140002526..140095397hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3892872
hg1992872
hg1892872
hg1792872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681808, nssv654872, nssv654381
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516840
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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