A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085821



Internal ID20652861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21727580..21728331hg38UCSC Ensembl
chr2:21950452..21951203hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085821
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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