A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1839155



Internal ID17745080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32944835..32946503hg38UCSC Ensembl
Innerchr10:33233763..33235431hg19UCSC Ensembl
Innerchr10:33273769..33275437hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381669
hg191669
hg181669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947823
Supporting Variants
SamplesHGDP00521
Known GenesITGB1
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)nssv1839155
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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