A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565631



Internal ID16006354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95320320..95666158hg38UCSC Ensembl
Innerchr14:95786657..96132495hg19UCSC Ensembl
Innerchr14:94856410..95202248hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38345839
hg19345839
hg18345839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832706
Samples
Known GenesGLRX5, LINC00341, SCARNA13, SNHG10, SYNE3, TCL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565631
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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