A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485139



Internal ID21142692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96190889..96191509hg38UCSC Ensembl
chr13:96843143..96843763hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015588
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485139
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