A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18078155



Internal ID20645195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144652501..144655800hg38UCSC Ensembl
chr2:145410068..145413367hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18078155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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