A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974582



Internal ID18263107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58150028..58155866hg38UCSC Ensembl
Innerchr15:58442227..58448065hg19UCSC Ensembl
Innerchr15:56229519..56235357hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385839
hg195839
hg185839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2026353, nssv2026357, nssv2026360, nssv2026358, nssv2026355, nssv2026352, nssv2026356, nssv2026359, nssv2026354, nssv2026351
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAQP9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974582
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