A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950990



Internal ID17299864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:88061344..88072143hg38UCSC Ensembl
Outerchr10:89821101..89831900hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998022
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950990
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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