A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090509



Internal ID20657549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:99144659..99152659hg38UCSC Ensembl
chr2:99761122..99769122hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350469
Supporting Variants
Samples
Known GenesC2orf15, TSGA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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