A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423020



Internal ID21080573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4665528..4706823hg38UCSC Ensembl
chr9:4665528..4706823hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841296
hg1941296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189862
Samples
Known GenesCDC37L1, SPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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