A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916265



Internal ID22691484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60396637..60397325hg38UCSC Ensembl
chr11:60164110..60164798hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351750
Samples
Known GenesMS4A14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916265
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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