A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421047



Internal ID21078600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23627455..23633758hg38UCSC Ensembl
chr9:23627453..23633756hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg386304
hg196304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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