A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2628025



Internal ID17771278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11926165..11927805hg38UCSC Ensembl
Innerchr16:12020022..12021662hg19UCSC Ensembl
Innerchr16:11927523..11929163hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg381641
hg191641
hg181641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv984258
Supporting Variants
SamplesHGDP00542
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2628025
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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