A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189273



Internal ID20756313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97322991..97323358hg38UCSC Ensembl
chr9:100085273..100085640hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445644
Supporting Variants
Samples
Known GenesCCDC180, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0006


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