A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139688



Internal ID20706728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132207659..132211588hg38UCSC Ensembl
chr6:132528799..132532728hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383930
hg193930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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