A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491288



Internal ID21148841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110877012..110878887hg38UCSC Ensembl
chr13:111529359..111531234hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381876
hg191876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007354
Samples
Known GenesANKRD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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