A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570242



Internal ID16357651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82078275..82117386hg38UCSC Ensembl
Innerchr15:82370616..82409727hg19UCSC Ensembl
Innerchr15:80157671..80196782hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3839112
hg1939112
hg1839112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847558
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570242
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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