A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950993



Internal ID17299867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91478144..91489843hg38UCSC Ensembl
Outerchr10:93237901..93249600hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998025
SamplesBILGI_BIOE
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950993
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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