A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493216



Internal ID21150769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90874180..91050049hg38UCSC Ensembl
chr13:91526434..91702303hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38175870
hg19175870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014616
Samples
Known GenesLINC00410
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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