A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519275



Internal ID15446568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166789305..166797813hg38UCSC Ensembl
Innerchr1:166758542..166767050hg19UCSC Ensembl
Innerchr1:165025166..165033674hg18UCSC Ensembl
Innerchr1:163490200..163498708hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg388509
hg198509
hg188509
hg178509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673387, nssv655163, nssv689533, nssv671803, nssv691052, nssv661096, nssv698745
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519275
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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