A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2613009



Internal ID17493838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49990996..49992151hg38UCSC Ensembl
Innerchr10:51750756..51751911hg19UCSC Ensembl
Innerchr10:51420762..51421917hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg381156
hg191156
hg181156
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971762
Supporting Variants
SamplesHGDP00998
Known GenesAGAP6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2613009
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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