A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060289



Internal ID20627329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25214023..25215071hg38UCSC Ensembl
chr1:25540514..25541562hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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