A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182275



Internal ID20749315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97318863..97340961hg38UCSC Ensembl
chr9:100081145..100103243hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3822099
hg1922099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439997
Supporting Variants
Samples
Known GenesCCDC180, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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