A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392569



Internal ID21050122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148921801..149089100hg38UCSC Ensembl
chr4:149842953..150010252hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38167300
hg19167300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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