A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978780



Internal ID18613983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15606825..15612857hg38UCSC Ensembl
Innerchr19:15717636..15723668hg19UCSC Ensembl
Innerchr19:15578636..15584668hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg386033
hg196033
hg186033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2136396, nssv2136391, nssv2136397, nssv2136400, nssv2136393, nssv2136392, nssv2136394, nssv2136395, nssv2136399, nssv2136398
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)nsv978780
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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