A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988221



Internal ID20555261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133930601..133932000hg38UCSC Ensembl
chr11:133800496..133801895hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457134
Supporting Variants
Samples
Known GenesIGSF9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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