A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490806



Internal ID21148359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91635202..91646481hg38UCSC Ensembl
chr13:92287456..92298735hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3811280
hg1911280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014694
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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