A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072088



Internal ID20639128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30193901..30277000hg38UCSC Ensembl
chr21:31566219..31649318hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3883100
hg1983100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537082
Supporting Variants
Samples
Known GenesCLDN8, LINC00307
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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