A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525769



Internal ID15106376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76340146..76369584hg38UCSC Ensembl
Innerchr15:76632487..76661925hg19UCSC Ensembl
Innerchr15:74419542..74448980hg18UCSC Ensembl
Innerchr15:74419542..74448980hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3829439
hg1929439
hg1829439
hg1729439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701937
Samples
Known GenesISL2, SCAPER
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525769
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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