A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958266



Internal ID17307139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:2512231..2512376hg38UCSC Ensembl
Outerchr5:2512345..2512490hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002202
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958266
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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