A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18086544



Internal ID20653584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230944881..230954372hg38UCSC Ensembl
chr2:231809596..231819087hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg389492
hg199492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345727
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18086544
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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