A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071544



Internal ID20638584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41681403..41684909hg38UCSC Ensembl
chr21:43101563..43105069hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg383507
hg193507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536755
Supporting Variants
Samples
Known GenesLINC00111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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