A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050398



Internal ID20617438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104993348..105004017hg38UCSC Ensembl
chr1:105535970..105546639hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3810670
hg1910670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050398
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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