A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1763336



Internal ID17795135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21399201..21431589hg38UCSC Ensembl
Innerchr1:21725694..21758082hg19UCSC Ensembl
Innerchr1:21598281..21630669hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3832389
hg1932389
hg1832389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945812
Supporting Variants
SamplesHGDP00778
Known Genes
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)nssv1763336
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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