A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064084



Internal ID20631124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76055573..76057424hg38UCSC Ensembl
chr1:76521258..76523109hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381852
hg191852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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