A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563772



Internal ID16351181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734966..19956348hg38UCSC Ensembl
Innerchr14:20203125..20424507hg19UCSC Ensembl
Innerchr14:19272965..19494347hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38221383
hg19221383
hg18221383
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821616, nssv821614, nssv821617, nssv821624, nssv821622, nssv821618, nssv821619, nssv821615, nssv821621, nssv821620, nssv821625, nssv821623
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)nsv563772
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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