A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963018



Internal ID18598260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18284802..18288501hg38UCSC Ensembl
Innerchr19:18395612..18399311hg19UCSC Ensembl
Innerchr19:18256612..18260311hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383700
hg193700
hg183700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2138018, nssv2138020, nssv2138017, nssv2138015, nssv2138016, nssv2138014, nssv2138021, nssv2138013, nssv2138022, nssv2138019
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)nsv963018
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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