A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961191



Internal ID18596437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15336703..15345170hg38UCSC Ensembl
Innerchr19:15447514..15455981hg19UCSC Ensembl
Innerchr19:15308514..15316981hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg388468
hg198468
hg188468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2135781, nssv2135777, nssv2135776, nssv2135772, nssv2135774, nssv2135773, nssv2135775, nssv2135779, nssv2135780, nssv2135778
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)nsv961191
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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