A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071581



Internal ID20638621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12698688..12699024hg38UCSC Ensembl
chrUn_gl000235:6958..7294hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.79253


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