A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2080954



Internal ID17767685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15698007..15706307hg38UCSC Ensembl
Innerchr17:15601321..15609621hg19UCSC Ensembl
Innerchr17:15542046..15550346hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg388301
hg198301
hg188301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv962262
Supporting Variants
SamplesHGDP00542
Known GenesZNF286A
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)nssv2080954
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