A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951521



Internal ID17300395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68233085..68303184hg38UCSC Ensembl
Outerchr9:70848001..70918100hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3870100
hg1970100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996900
SamplesBILGI_BIOE
Known GenesCBWD3, CBWD5, FOXD4L3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951521
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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