A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490791



Internal ID21148344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57693900..57694471hg38UCSC Ensembl
chr13:58268034..58268605hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011458
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490791
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