A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570907



Internal ID16011630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101663675..101733297hg38UCSC Ensembl
Innerchr15:102203878..102273500hg19UCSC Ensembl
Innerchr15:100021401..100091023hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3869623
hg1969623
hg1869623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4800n54
Supporting Variantsnssv851212
Samples
Known GenesTARSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570907
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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