A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955742



Internal ID17304615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:50110091..50144938hg38UCSC Ensembl
Outerchr5:49405925..49440772hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3834848
hg1934848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002033
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955742
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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