A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486157



Internal ID21143710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63186101..63187000hg38UCSC Ensembl
chr13:63760234..63761133hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486157
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