A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977663



Internal ID18612869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22519558..22524713hg38UCSC Ensembl
Innerchr15:23348383..23353538hg19UCSC Ensembl
Innerchr15:20899824..20904979hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg385156
hg195156
hg185156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2007716, nssv2007719, nssv2007718, nssv2007721, nssv2007720, nssv2007717, nssv2007715, nssv2007714, nssv2007722, nssv2007723
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHERC2P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977663
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