A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424761



Internal ID21082314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3692648..3720409hg38UCSC Ensembl
chr9:3692648..3720409hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3827762
hg1927762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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