A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479375



Internal ID21136928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94132405..94132955hg38UCSC Ensembl
chr13:94784659..94785209hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015331
Samples
Known GenesGPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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