A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414763



Internal ID21072316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81899928..81902398hg38UCSC Ensembl
chr5:81195747..81198217hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg382471
hg192471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414763
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