A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180351



Internal ID20747391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97958501..97963900hg38UCSC Ensembl
chr15:98501731..98507130hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505231
Supporting Variants
Samples
Known GenesARRDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180351
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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