A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977470



Internal ID18265990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55391926..55395595hg38UCSC Ensembl
Innerchr14:55858644..55862313hg19UCSC Ensembl
Innerchr14:54928397..54932066hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg383670
hg193670
hg183670
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1987102, nssv1987103, nssv1987108, nssv1987106, nssv1987099, nssv1987101, nssv1987104, nssv1987105, nssv1987107, nssv1987100
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesATG14
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977470
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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