A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483652



Internal ID21141205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58534560..58548489hg38UCSC Ensembl
chr13:59108694..59122623hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3813930
hg1913930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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