A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039002



Internal ID20606042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77372380..77372820hg38UCSC Ensembl
chr17:75368462..75368902hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528804
Supporting Variants
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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