A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425518



Internal ID21083071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14654998..14655528hg38UCSC Ensembl
chr9:14654996..14655526hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174976
Samples
Known GenesZDHHC21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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