A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974617



Internal ID18609828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85169256..85272121hg38UCSC Ensembl
Innerchr15:85712487..85815352hg19UCSC Ensembl
Innerchr15:83513491..83616356hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38102866
hg19102866
hg18102866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2035836, nssv2035834, nssv2035841, nssv2035833, nssv2035839, nssv2035838, nssv2035835, nssv2035837, nssv2035840, nssv2035832
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC440300, LOC642423
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974617
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