A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528784



Internal ID15456077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:69897656..69902679hg38UCSC Ensembl
Innerchr15:70189995..70195018hg19UCSC Ensembl
Innerchr15:67977049..67982072hg18UCSC Ensembl
Innerchr15:67977049..67982072hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385024
hg195024
hg185024
hg175024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705451
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528784
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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