A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1837018



Internal ID17794497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32102230..32103230hg38UCSC Ensembl
Innerchr10:32391158..32392158hg19UCSC Ensembl
Innerchr10:32431164..32432164hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947820
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)nssv1837018
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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