A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099721



Internal ID20666761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177663401..177666500hg38UCSC Ensembl
chr3:177381189..177384288hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362300
Supporting Variants
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.09468


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