A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992504



Internal ID20559544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60396638..60397326hg38UCSC Ensembl
chr11:60164111..60164799hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458827
Supporting Variants
Samples
Known GenesMS4A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992504
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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