A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071981



Internal ID20639021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33606926..33607547hg38UCSC Ensembl
chr21:34979232..34979853hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550805
Supporting Variants
Samples
Known GenesCRYZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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