A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976955



Internal ID18612161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79556484..79560451hg38UCSC Ensembl
Innerchr15:79848826..79852793hg19UCSC Ensembl
Innerchr15:77635881..77639848hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383968
hg193968
hg183968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2033782, nssv2033781, nssv2033788, nssv2033787, nssv2033790, nssv2033785, nssv2033783, nssv2033786, nssv2033784, nssv2033789
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976955
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