A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961171



Internal ID18596417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9102950..9106855hg38UCSC Ensembl
Innerchr19:9213626..9217531hg19UCSC Ensembl
Innerchr19:9074626..9078531hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383906
hg193906
hg183906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2129834, nssv2129830, nssv2129831, nssv2129833, nssv2129827, nssv2129828, nssv2129832, nssv2129825, nssv2129826, nssv2129829
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7G2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961171
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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