A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569403



Internal ID16010126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50899224..51012176hg38UCSC Ensembl
Innerchr15:51191421..51304373hg19UCSC Ensembl
Innerchr15:48978713..49091665hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38112953
hg19112953
hg18112953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842978
Samples
Known GenesAP4E1, DCAF13P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569403
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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