A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570357



Internal ID16011080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:86338430..86371858hg38UCSC Ensembl
Innerchr15:86881661..86915089hg19UCSC Ensembl
Innerchr15:84682665..84716093hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3833429
hg1933429
hg1833429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149258
Samples1787431198_A
Known GenesAGBL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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