A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961179



Internal ID18596425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12185706..12186434hg38UCSC Ensembl
Innerchr19:12296521..12297249hg19UCSC Ensembl
Innerchr19:12157521..12158249hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38729
hg19729
hg18729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2133000, nssv2133004, nssv2133005, nssv2133006, nssv2133003, nssv2133008, nssv2133002, nssv2133007, nssv2133009, nssv2133001
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF136
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961179
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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