A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039010



Internal ID20606050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77495727..77496628hg38UCSC Ensembl
chr17:75491809..75492710hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526305
Supporting Variants
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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