A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178513



Internal ID20745553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34628501..34629300hg38UCSC Ensembl
chr9:34628498..34629297hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443613
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.033


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