A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091148



Internal ID20658188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85713738..85717813hg38UCSC Ensembl
chr2:85940861..85944936hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg384076
hg194076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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