A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489214



Internal ID21146767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73559861..73560284hg38UCSC Ensembl
chr13:74133998..74134421hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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