A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419723



Internal ID21077276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15157390..15159634hg38UCSC Ensembl
chr9:15157388..15159632hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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