A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1834006



Internal ID17777836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24583816..24586115hg38UCSC Ensembl
Innerchr10:24872745..24875044hg19UCSC Ensembl
Innerchr10:24912751..24915050hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg382300
hg192300
hg182300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947769
Supporting Variants
SamplesHGDP00665
Known GenesARHGAP21
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)nssv1834006
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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