A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977489



Internal ID18612695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76633879..76635572hg38UCSC Ensembl
Innerchr14:77100222..77101915hg19UCSC Ensembl
Innerchr14:76169975..76171668hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381694
hg191694
hg181694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1991991, nssv1991990, nssv1991984, nssv1991983, nssv1991985, nssv1991982, nssv1991989, nssv1991987, nssv1991988, nssv1991986
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977489
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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