A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178759



Internal ID20745799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82317801..82322500hg38UCSC Ensembl
chr15:82610137..82614836hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495907
Supporting Variants
Samples
Known GenesADAMTS7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178759
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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