A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565779



Internal ID16006502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100238360..100240636hg38UCSC Ensembl
Innerchr14:100704697..100706973hg19UCSC Ensembl
Innerchr14:99774450..99776726hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382277
hg192277
hg182277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3897n54
Supporting Variantsnssv833073
Samples
Known GenesYY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565779
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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