A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476816



Internal ID21134369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75530699..75531227hg38UCSC Ensembl
chr13:76104835..76105363hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18013357
Samples
Known GenesCOMMD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476816
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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