A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985108



Internal ID20552148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100805738..100809276hg38UCSC Ensembl
chr11:100676469..100680007hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383539
hg193539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457385
Supporting Variants
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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