A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977457



Internal ID18612663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35429999..35432532hg38UCSC Ensembl
Innerchr14:35899205..35901738hg19UCSC Ensembl
Innerchr14:34968956..34971489hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382534
hg192534
hg182534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1984095, nssv1984098, nssv1984101, nssv1984100, nssv1984103, nssv1984096, nssv1984104, nssv1984102, nssv1984099, nssv1984097
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)nsv977457
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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