A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125956



Internal ID20692996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14872308..14878170hg38UCSC Ensembl
chr5:14872417..14878279hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385863
hg195863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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