A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057260



Internal ID20624300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:209536701..209543600hg38UCSC Ensembl
chr1:209710046..209716945hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330241
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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