A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223232



Internal ID20790272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93265661..93357205hg38UCSC Ensembl
chr9:96027943..96119487hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3891545
hg1991545
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453736
Supporting Variants
Samples
Known GenesC9orf129, WNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223232
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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