A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191057



Internal ID20758097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94716858..94735359hg38UCSC Ensembl
chr9:97479140..97497641hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3818502
hg1918502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436782
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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