A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363985



Internal ID21021538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22553078..22553934hg38UCSC Ensembl
chr4:22554701..22555557hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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