A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1862802



Internal ID17812252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91052926..91056046hg38UCSC Ensembl
Innerchr10:92812683..92815803hg19UCSC Ensembl
Innerchr10:92802663..92805783hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg383121
hg193121
hg183121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948133
Supporting Variants
SamplesHGDP00927
Known GenesLINC00502
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)nssv1862802
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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