A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960267



Internal ID18595520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15163005..15381175hg38UCSC Ensembl
Innerchr18:15163004..15381174hg19UCSC Ensembl
Innerchr18:15153004..15371174hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38218171
hg19218171
hg18218171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2120680, nssv2119880, nssv2120679, nssv2119881, nssv2120677, nssv2120678, nssv2119883, nssv2120681, nssv2119882, nssv2120676
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC644669
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960267
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer