A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522166



Internal ID15449459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58331209..58332129hg38UCSC Ensembl
Innerchr15:58623408..58624328hg19UCSC Ensembl
Innerchr15:56410700..56411620hg18UCSC Ensembl
Innerchr15:56410700..56411620hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38921
hg19921
hg18921
hg17921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694939
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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