A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519365



Internal ID15446658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88132435..88151979hg38UCSC Ensembl
Innerchr6:88842154..88861698hg19UCSC Ensembl
Innerchr6:88898873..88918417hg18UCSC Ensembl
Innerchr6:88898873..88918417hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3819545
hg1919545
hg1819545
hg1719545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672540, nssv677824, nssv655820, nssv655655, nssv663742
Samples
Known GenesCNR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519365
Frequency
Sample Size2026
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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