A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519791



Internal ID15447084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95976306..95979742hg38UCSC Ensembl
Innerchr6:96424182..96427618hg19UCSC Ensembl
Innerchr6:96530903..96534339hg18UCSC Ensembl
Innerchr6:96530903..96534339hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg383437
hg193437
hg183437
hg173437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697053
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519791
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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