A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950622



Internal ID17299496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:661486..693585hg38UCSC Ensembl
Outerchr5:661601..693700hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3832100
hg1932100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997680
SamplesBILGI_BIOE
Known GenesTPPP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950622
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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