A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102149



Internal ID20669189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37430212..37439288hg38UCSC Ensembl
chr3:37471703..37480779hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg389077
hg199077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370973
Supporting Variants
Samples
Known GenesC3orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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