A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374700



Internal ID21032253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14774513..14776022hg38UCSC Ensembl
chr3:14816020..14817529hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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