A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385417



Internal ID21042970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163093301..163095700hg38UCSC Ensembl
chr4:164014453..164016852hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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