A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362500



Internal ID21020053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16292501..16302100hg38UCSC Ensembl
chr4:16294124..16303723hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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