A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994946



Internal ID20561986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87465018..87473874hg38UCSC Ensembl
chr11:87176060..87184916hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg388857
hg198857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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