A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18085657



Internal ID20652697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26235255..26241536hg38UCSC Ensembl
chr2:26458123..26464404hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg386282
hg196282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6340989
Supporting Variants
Samples
Known GenesHADHA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18085657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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