A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487449



Internal ID21145002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58135165..58191708hg38UCSC Ensembl
chr13:58709299..58765842hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3856544
hg1956544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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