A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190726



Internal ID20757766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41232267..41301450hg38UCSC Ensembl
chr15:41524465..41593648hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3869184
hg1969184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499995
Supporting Variants
Samples
Known GenesCHP1, OIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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