A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187069



Internal ID20754109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38097993..38143742hg38UCSC Ensembl
chr13:38672130..38717879hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3845750
hg1945750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489375
Supporting Variants
Samples
Known GenesLINC00571
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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