A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522748



Internal ID15450041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37259056..37268588hg38UCSC Ensembl
Innerchr15:37551257..37560789hg19UCSC Ensembl
Innerchr15:35338549..35348081hg18UCSC Ensembl
Innerchr15:35338549..35348081hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg389533
hg199533
hg189533
hg179533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698383
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522748
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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