A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368029



Internal ID21025582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5592784..5599385hg38UCSC Ensembl
chr4:5594511..5601112hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg386602
hg196602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118396
Samples
Known GenesEVC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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