A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563760



Internal ID16351169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19728059..19955745hg38UCSC Ensembl
Innerchr14:20196218..20423904hg19UCSC Ensembl
Innerchr14:19266058..19493744hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38227687
hg19227687
hg18227687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821577, nssv821579, nssv821576, nssv821578, nssv821575
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)nsv563760
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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