A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977487



Internal ID18612693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74902403..74903494hg38UCSC Ensembl
Innerchr14:75369106..75370197hg19UCSC Ensembl
Innerchr14:74438859..74439950hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381092
hg191092
hg181092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1993799, nssv1993795, nssv1993792, nssv1993797, nssv1993801, nssv1993796, nssv1993798, nssv1993794, nssv1993800, nssv1993793
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDLST
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977487
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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