A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384969



Internal ID21042522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2124823..2125899hg38UCSC Ensembl
chr5:2124937..2126013hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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