A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463900



Internal ID22521786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60169088..60214831hg38UCSC Ensembl
chr11:59936561..59982304hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3845744
hg1945744
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848733
Supporting Variants
Samples
Known GenesMS4A6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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