A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974367



Internal ID18609578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92763839..92768716hg38UCSC Ensembl
Innerchr14:93230184..93235061hg19UCSC Ensembl
Innerchr14:92299937..92304814hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg384878
hg194878
hg184878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1996303, nssv1996308, nssv1996306, nssv1996301, nssv1996299, nssv1996305, nssv1996307, nssv1996302, nssv1996300, nssv1996304
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)nsv974367
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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