A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023953



Internal ID21933296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94106053..94106143hg38UCSC Ensembl
chr13:94758307..94758397hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602933
Samples
Known GenesGPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023953
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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