A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069724



Internal ID20636764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30500550..30520739hg38UCSC Ensembl
chr21:31872868..31893057hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3820190
hg1920190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544088
Supporting Variants
Samples
Known GenesKRTAP19-5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069724
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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