A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2007625



Internal ID17785464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22533639..22565685hg38UCSC Ensembl
Innerchr15:23307411..23339457hg19UCSC Ensembl
Innerchr15:20858852..20890898hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3832047
hg1932047
hg1832047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974525
Supporting Variants
SamplesHGDP00665
Known GenesHERC2P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2007625
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer