A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977491



Internal ID18612697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76967201..76969117hg38UCSC Ensembl
Innerchr14:77433544..77435460hg19UCSC Ensembl
Innerchr14:76503297..76505213hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381917
hg191917
hg181917
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1992976, nssv1992968, nssv1992971, nssv1992975, nssv1992969, nssv1992972, nssv1992970, nssv1992974, nssv1992973, nssv1992977
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)nsv977491
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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