A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070623



Internal ID20637663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7468117..7472041hg38UCSC Ensembl
chr20:7448764..7452688hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg383925
hg193925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516146
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070623
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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