A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995027



Internal ID20562067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88224001..88230000hg38UCSC Ensembl
chr11:87957169..87963168hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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