A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065402



Internal ID20632442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11728302..11728519hg38UCSC Ensembl
chr20:11708950..11709167hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0015


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