A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1862890



Internal ID17878606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91464254..91479296hg38UCSC Ensembl
Innerchr10:93224011..93239053hg19UCSC Ensembl
Innerchr10:93213991..93229033hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3815043
hg1915043
hg1815043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv948134
Supporting Variants
SamplesHGDP01307
Known GenesHECTD2, LOC100188947
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)nssv1862890
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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