A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366859



Internal ID21024412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17541401..17568000hg38UCSC Ensembl
chr4:17543024..17569623hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3826600
hg1926600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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