A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951175



Internal ID17300049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:62491900..62596799hg38UCSC Ensembl
Outerchr9:46803201..46908100hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38104900
hg19104900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999484
SamplesBILGI_BIOE
Known GenesLOC643648
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951175
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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