A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961173



Internal ID18596419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9190424..9192265hg38UCSC Ensembl
Innerchr19:9301100..9302941hg19UCSC Ensembl
Innerchr19:9162100..9163941hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381842
hg191842
hg181842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2130818, nssv2130819, nssv2130811, nssv2130814, nssv2130817, nssv2130813, nssv2130820, nssv2130812, nssv2130815, nssv2130816
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)nsv961173
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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