A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203633



Internal ID20770673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35170868..35183340hg38UCSC Ensembl
chr1:35636469..35648941hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812473
hg1912473
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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