A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064781



Internal ID20631821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85013191..85013577hg38UCSC Ensembl
chr1:85478874..85479260hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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