A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950448



Internal ID17299322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:174299698..174321297hg38UCSC Ensembl
Outerchr5:173726701..173748300hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3821600
hg1921600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997881
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950448
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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