A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185485



Internal ID20752525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81541764..81566776hg38UCSC Ensembl
chr17:79508790..79533802hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3825013
hg1925013
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534585
Supporting Variants
Samples
Known GenesC17orf70, NPLOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185485
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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