A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200633



Internal ID20767673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:242546008..242570427hg38UCSC Ensembl
chr1:242709310..242733729hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3824420
hg1924420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330332
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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