A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568664



Internal ID16356073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27903455..27992763hg38UCSC Ensembl
Innerchr15:28148601..28237909hg19UCSC Ensembl
Innerchr15:25822196..25911504hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3889309
hg1989309
hg1889309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149546
Samples1780854417_A
Known GenesOCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568664
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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