A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188109



Internal ID20755149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75554284..75575875hg38UCSC Ensembl
chr17:73550365..73571956hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3821592
hg1921592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526711
Supporting Variants
Samples
Known GenesLLGL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188109
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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