A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360895



Internal ID21018448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76318248..76318622hg38UCSC Ensembl
chr3:76367399..76367773hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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