A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191194



Internal ID20758234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56838307..56921338hg38UCSC Ensembl
chr15:57130505..57213536hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3883032
hg1983032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507887
Supporting Variants
Samples
Known GenesLOC145783, TCF12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191194
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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