A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486748



Internal ID21144301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68218355..68231223hg38UCSC Ensembl
chr13:68792487..68805355hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812869
hg1912869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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