A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2019063



Internal ID17801209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40125026..40135151hg38UCSC Ensembl
Innerchr15:40417227..40427352hg19UCSC Ensembl
Innerchr15:38204519..38214644hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810126
hg1910126
hg1810126
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv974562
Supporting Variants
SamplesHGDP00778
Known Genes
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)nssv2019063
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