A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125165



Internal ID20692205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140685566..140689696hg38UCSC Ensembl
chr5:140065151..140069281hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg384131
hg194131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405798
Supporting Variants
Samples
Known GenesHARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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