A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18081723



Internal ID20648763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183865521..183935202hg38UCSC Ensembl
chr2:184730248..184799929hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3869682
hg1969682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353584
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18081723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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