A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177848



Internal ID20744888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33176448..33176916hg38UCSC Ensembl
chr9:33176446..33176914hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452364
Supporting Variants
Samples
Known GenesLOC101929639
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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