A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089113



Internal ID20656153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37850891..37853981hg38UCSC Ensembl
chr2:38078034..38081124hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg383091
hg193091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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