A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191354



Internal ID20758395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77302025..77315138hg38UCSC Ensembl
chr17:75298107..75311220hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3813114
hg1913114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533860
Supporting Variants
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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