A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565773



Internal ID16006496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100235080..100240715hg38UCSC Ensembl
Innerchr14:100701417..100707052hg19UCSC Ensembl
Innerchr14:99771170..99776805hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385636
hg195636
hg185636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3895n54
Supporting Variantsnssv833067
Samples
Known GenesYY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565773
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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