A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190205



Internal ID20757245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96383301..96384000hg38UCSC Ensembl
chr9:99145583..99146282hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445239
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08018


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