A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201466



Internal ID20768506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53988281..54067983hg38UCSC Ensembl
chr1:54453954..54533656hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3879703
hg1979703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331104
Supporting Variants
Samples
Known GenesLDLRAD1, MIR4781, TCEANC2, TMEM59
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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