A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091147



Internal ID20658187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85707646..85707989hg38UCSC Ensembl
chr2:85934769..85935112hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00225


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