A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516009



Internal ID15443066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21728086..21740651hg38UCSC Ensembl
Innerchr6:21728317..21740882hg19UCSC Ensembl
Innerchr6:21836296..21848861hg18UCSC Ensembl
Innerchr6:21836296..21848861hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3812566
hg1912566
hg1812566
hg1712566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667037, nssv665698
Samples
Known GenesCASC15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516009
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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