A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18084442



Internal ID20651482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238508264..238511290hg38UCSC Ensembl
chr2:239416905..239419931hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383027
hg193027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335651
Supporting Variants
Samples
Known GenesLINC01107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18084442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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