A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182405



Internal ID20749445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41476002..41489229hg38UCSC Ensembl
chr15:41768200..41781427hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3813228
hg1913228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506803
Supporting Variants
Samples
Known GenesRTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182405
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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