A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521153



Internal ID15448446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164865904..164930068hg38UCSC Ensembl
Innerchr6:165279393..165343557hg19UCSC Ensembl
Innerchr6:165199383..165263547hg18UCSC Ensembl
Innerchr6:165249804..165313968hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3864165
hg1964165
hg1864165
hg1764165
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683109, nssv701001, nssv693520
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521153
Frequency
Sample Size2026
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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