A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360918



Internal ID21018471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63816832..63818539hg38UCSC Ensembl
chr3:63802508..63804215hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360918
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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