A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176985



Internal ID20744025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131543025..131570913hg38UCSC Ensembl
chr9:134418412..134446300hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3827889
hg1927889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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