A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414474



Internal ID21072027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65545591..65547998hg38UCSC Ensembl
chr5:64841418..64843825hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382408
hg192408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133241
Samples
Known GenesCENPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414474
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