A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192121



Internal ID20759161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39571298..39650813hg38UCSC Ensembl
chr15:39863499..39943014hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3879516
hg1979516
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508798
Supporting Variants
Samples
Known GenesFSIP1, THBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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