A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203072



Internal ID20770112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39035419..39077967hg38UCSC Ensembl
chr1:39501091..39543639hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3842549
hg1942549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329303
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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