A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952119



Internal ID16954306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:7700483..7709982hg38UCSC Ensembl
Outerchr17:7603801..7613300hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000238
SamplesBILGI_BIOE
Known GenesEFNB3, WRAP53
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952119
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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