A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998061



Internal ID17291013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118726289..118738188hg38UCSC Ensembl
Outerchr10:120485801..120497700hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951862
Supporting Variants
SamplesBILGI_BIOE
Known GenesCACUL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998061
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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