A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2426632



Internal ID17842556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149593935..149594527hg38UCSC Ensembl
Innerchr6:149915071..149915663hg19UCSC Ensembl
Innerchr6:149956764..149957356hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38593
hg19593
hg18593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv970171
Supporting Variants
SamplesHGDP00998
Known GenesRPS18P9
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)nssv2426632
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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