A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364635



Internal ID21022188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13852392..13853055hg38UCSC Ensembl
chr4:13854016..13854679hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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