A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442704



Internal ID21100257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87583304..87598180hg38UCSC Ensembl
chr9:90198219..90213095hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3814877
hg1914877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191161
Samples
Known GenesDAPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442704
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