A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203111



Internal ID20770151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41041198..41041654hg38UCSC Ensembl
chr1:41506870..41507326hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335419
Supporting Variants
Samples
Known GenesSCMH1, SLFNL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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