A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202089



Internal ID20769130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58463715..59072395hg38UCSC Ensembl
chr1:58929387..59538067hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38608681
hg19608681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317998
Supporting Variants
Samples
Known GenesJUN, LINC01135, MYSM1, OMA1, TACSTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202089
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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