A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495432



Internal ID21152985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91088308..91094469hg38UCSC Ensembl
chr13:91740562..91746723hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg386162
hg196162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014637
Samples
Known GenesLINC00380
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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