A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385003



Internal ID21042556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161304636..161314165hg38UCSC Ensembl
chr4:162225788..162235317hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg389530
hg199530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113667
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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