A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570596



Internal ID16358005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97267472..97311580hg38UCSC Ensembl
Innerchr15:97810702..97854810hg19UCSC Ensembl
Innerchr15:95611706..95655814hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3844109
hg1944109
hg1844109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4747n54
Supporting Variantsnssv849147
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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