A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175196



Internal ID20742236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129322267..129324112hg38UCSC Ensembl
chr9:132084546..132086391hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381846
hg191846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453525
Supporting Variants
Samples
Known GenesC9orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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