A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955834



Internal ID17304707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:36357223..36357470hg38UCSC Ensembl
Outerchr5:36357325..36357572hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002147
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955834
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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