A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176524



Internal ID20743564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123120042..123120354hg38UCSC Ensembl
chr9:125882321..125882633hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176524
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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