A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565044



Internal ID16005767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:71851244..71869425hg38UCSC Ensembl
Innerchr14:72317961..72336142hg19UCSC Ensembl
Innerchr14:71387714..71405895hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3818182
hg1918182
hg1818182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829091
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565044
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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