A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191141



Internal ID20758181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75624243..75642385hg38UCSC Ensembl
chr15:75916584..75934726hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3818143
hg1918143
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498618
Supporting Variants
Samples
Known GenesIMP3, SNUPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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