A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570173



Internal ID16357582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77818881..77819586hg38UCSC Ensembl
Innerchr15:78111223..78111928hg19UCSC Ensembl
Innerchr15:75898278..75898983hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv847381, nssv847380, nssv847379
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570173
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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