A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089928



Internal ID20656968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4127587..4171270hg38UCSC Ensembl
chr2:4175178..4218860hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3843684
hg1943683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353264
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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