A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477496



Internal ID21135049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94172956..94203071hg38UCSC Ensembl
chr13:94825210..94855325hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3830116
hg1930116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015336
Samples
Known GenesGPC6, GPC6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer