A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062984



Internal ID20630024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75220866..75231209hg38UCSC Ensembl
chr1:75686551..75696894hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3810344
hg1910344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331879
Supporting Variants
Samples
Known GenesSLC44A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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