A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983801



Internal ID18618993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19862679..19956757hg38UCSC Ensembl
Innerchr14:20330838..20424916hg19UCSC Ensembl
Innerchr14:19400678..19494756hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3894079
hg1994079
hg1894079
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763417, nssv2757059, nssv2766102
SamplesHGDP01284, HGDP00665, HGDP00778
Known GenesOR4K1, OR4K2, OR4K5
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983801
Frequency
Sample Size10
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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