A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961172



Internal ID18596418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9126526..9128320hg38UCSC Ensembl
Innerchr19:9237202..9238996hg19UCSC Ensembl
Innerchr19:9098202..9099996hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381795
hg191795
hg181795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2130720, nssv2130719, nssv2130716, nssv2130714, nssv2130717, nssv2130718, nssv2130723, nssv2130715, nssv2130721, nssv2130722
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR7G3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961172
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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