A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190636



Internal ID20757676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50324576..50331906hg38UCSC Ensembl
chr15:50616773..50624103hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg387331
hg197331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499298
Supporting Variants
Samples
Known GenesGABPB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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