A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2085884



Internal ID17785380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21321364..21352923hg38UCSC Ensembl
Innerchr17:21224676..21256235hg19UCSC Ensembl
Innerchr17:21165269..21196828hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3831560
hg1931560
hg1831560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv960443
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2085884
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