A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570628



Internal ID16358037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97273703..97314802hg38UCSC Ensembl
Innerchr15:97816933..97858032hg19UCSC Ensembl
Innerchr15:95617937..95659036hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3841100
hg1941100
hg1841100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4747n54
Supporting Variantsnssv849298
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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