A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075587



Internal ID21470951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60713898..60714222hg38UCSC Ensembl
chr11:60481371..60481695hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594743
Supporting Variants
SamplesHG03125
Known GenesMS4A8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075587
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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