A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091783



Internal ID20658823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8688364..8689028hg38UCSC Ensembl
chr2:8828494..8829158hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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