A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202032



Internal ID20769073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219468787..219489897hg38UCSC Ensembl
chr1:219642129..219663239hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3821111
hg1921111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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