A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2276467



Internal ID17781826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:31986079..31996187hg38UCSC Ensembl
Innerchr3:32027571..32037679hg19UCSC Ensembl
Innerchr3:32002575..32012683hg18UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg3810109
hg1910109
hg1810109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv967000
Supporting Variants
SamplesHGDP00665
Known GenesZNF860
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)nssv2276467
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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