A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102948



Internal ID20669988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58572598..58573319hg38UCSC Ensembl
chr3:58558325..58559046hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369164
Supporting Variants
Samples
Known GenesFAM107A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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