A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039009



Internal ID20606049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77494681..77495189hg38UCSC Ensembl
chr17:75490763..75491271hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38509
hg19509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520885
Supporting Variants
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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