A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565778



Internal ID16353187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100238205..100243293hg38UCSC Ensembl
Innerchr14:100704542..100709630hg19UCSC Ensembl
Innerchr14:99774295..99779383hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385089
hg195089
hg185089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833072
Samples
Known GenesYY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565778
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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