A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2432245



Internal ID17779567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170643424..170710693hg38UCSC Ensembl
Innerchr6:170952512..171019781hg19UCSC Ensembl
Innerchr6:170794437..170861706hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3867270
hg1967270
hg1867270
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv965673
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)nssv2432245
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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