A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409432



Internal ID21066985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166217601..166219200hg38UCSC Ensembl
chr5:165644606..165646205hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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