A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962991



Internal ID18598233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:190564..265805hg38UCSC Ensembl
Innerchr19:190564..265805hg19UCSC Ensembl
Innerchr19:141564..216805hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3875242
hg1975242
hg1875242
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2127571, nssv2127573, nssv2127580, nssv2127572, nssv2127577, nssv2127574, nssv2127579, nssv2127575, nssv2127576, nssv2127578
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC01002
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962991
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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