A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365480



Internal ID21023033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25220596..25221463hg38UCSC Ensembl
chr4:25222218..25223085hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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