A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569227



Internal ID16356636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40273504..40314283hg38UCSC Ensembl
Innerchr15:40565705..40606484hg19UCSC Ensembl
Innerchr15:38352997..38393776hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3840780
hg1940780
hg1840780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149587
SamplesNINDS_70
Known GenesANKRD63, PAK6, PLCB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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