A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373716



Internal ID21031269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19512250..19521953hg38UCSC Ensembl
chr4:19513873..19523576hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg389704
hg199704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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