A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960782



Internal ID18596029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7876264..7879899hg38UCSC Ensembl
Innerchr19:7941149..7944784hg19UCSC Ensembl
Innerchr19:7847149..7850784hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383636
hg193636
hg183636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2130265, nssv2130263, nssv2130259, nssv2130257, nssv2130262, nssv2130256, nssv2130260, nssv2130264, nssv2130258, nssv2130261
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC388499
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960782
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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