A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482603



Internal ID21140156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71789487..71789874hg38UCSC Ensembl
chr13:72363619..72364006hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012947
Samples
Known GenesDACH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482603
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