A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570360



Internal ID16357769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87245241..87319578hg38UCSC Ensembl
Innerchr15:87788472..87862809hg19UCSC Ensembl
Innerchr15:85589476..85663813hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3874338
hg1974338
hg1874338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4702n54
Supporting Variantsnssv1149259
SamplesNINDS_186
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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