A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357980



Internal ID21015533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75912973..75913527hg38UCSC Ensembl
chr3:75962124..75962678hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357980
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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