A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094972



Internal ID20662012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13701574..13718396hg38UCSC Ensembl
chr3:13743073..13759895hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3816823
hg1916823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374188
Supporting Variants
Samples
Known GenesLINC00620
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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