A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2010610



Internal ID17850318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28211180..28244658hg38UCSC Ensembl
Innerchr15:28456326..28489804hg19UCSC Ensembl
Innerchr15:26129921..26163399hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3833479
hg1933479
hg1833479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984035
Supporting Variants
SamplesHGDP01029
Known GenesHERC2
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)nssv2010610
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