A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495122



Internal ID21152675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61201624..61202129hg38UCSC Ensembl
chr13:61775758..61776263hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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