A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545557



Internal ID20918788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39345920..39349819hg38UCSC Ensembl
chr21:40717846..40721745hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18072390
Samples
Known GenesHMGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545557
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