A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180976



Internal ID20748016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88515017..88516505hg38UCSC Ensembl
chr9:91129932..91131420hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381489
hg191489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439704
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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