A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203602



Internal ID20770642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32404245..32449317hg38UCSC Ensembl
chr1:32869846..32914918hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3845073
hg1945073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320236
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203602
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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