A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071548



Internal ID20638588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41716782..41718447hg38UCSC Ensembl
chr21:43136942..43138607hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381666
hg191666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552933
Supporting Variants
Samples
Known GenesLINC00112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071548
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041


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