A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974620



Internal ID18609831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92709644..92715543hg38UCSC Ensembl
Innerchr15:93252874..93258773hg19UCSC Ensembl
Innerchr15:91053878..91059777hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg385900
hg195900
hg185900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2038103, nssv2038109, nssv2038108, nssv2038105, nssv2038102, nssv2038104, nssv2038107, nssv2038111, nssv2038106, nssv2038110
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)nsv974620
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