A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091153



Internal ID20658193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85807853..85809272hg38UCSC Ensembl
chr2:86034976..86036395hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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