A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024824



Internal ID21934167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113830496..113830648hg38UCSC Ensembl
chr13:114533469..114533621hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599927
Samples
Known GenesGAS6, GAS6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024824
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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