A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570143



Internal ID16357552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77700940..77725019hg38UCSC Ensembl
Innerchr15:77993282..78017361hg19UCSC Ensembl
Innerchr15:75780337..75804416hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3824080
hg1924080
hg1824080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4660n54
Supporting Variantsnssv847256
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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