A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2055858



Internal ID17833499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29629998..29637691hg38UCSC Ensembl
Innerchr16:29641319..29649012hg19UCSC Ensembl
Innerchr16:29548820..29556513hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387694
hg197694
hg187694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv974797
Supporting Variants
SamplesHGDP00998
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)nssv2055858
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