A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365543



Internal ID21023096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2429763..2438363hg38UCSC Ensembl
chr4:2431490..2440090hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg388601
hg198601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113343
Samples
Known GenesLOC402160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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