A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201840



Internal ID20768881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203750242..203779805hg38UCSC Ensembl
chr1:203719370..203748933hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3829564
hg1929564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322731
Supporting Variants
Samples
Known GenesLAX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201840
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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