A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565206



Internal ID16352615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76369614..76547692hg38UCSC Ensembl
Innerchr14:76835957..77014035hg19UCSC Ensembl
Innerchr14:75905710..76083788hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38178079
hg19178079
hg18178079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829557
Samples
Known GenesESRRB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565206
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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