A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563771



Internal ID16351180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19955745hg38UCSC Ensembl
Innerchr14:20203125..20423904hg19UCSC Ensembl
Innerchr14:19272965..19493744hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38220780
hg19220780
hg18220780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821613, nssv821612
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563771
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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