A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176797



Internal ID20743838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127294402..127299594hg38UCSC Ensembl
chr9:130056681..130061873hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385193
hg195193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455249
Supporting Variants
Samples
Known GenesGARNL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176797
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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