A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549280



Internal ID20922448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14372469..14373096hg38UCSC Ensembl
chr21:15744790..15745417hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068618
Samples
Known GenesHSPA13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549280
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