A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393424



Internal ID21050977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40251249..40253135hg38UCSC Ensembl
chr4:40252869..40254755hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381887
hg191887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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