A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364217



Internal ID21021770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9955682..9960394hg38UCSC Ensembl
chr3:9997366..10002078hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384713
hg194713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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