A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570581



Internal ID16011304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96330303..96331011hg38UCSC Ensembl
Innerchr15:96873532..96874240hg19UCSC Ensembl
Innerchr15:94674536..94675244hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38709
hg19709
hg18709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv849103, nssv849104
Samples
Known GenesNR2F2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570581
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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