A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3948185



Internal ID21368254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102601115..102601431hg38UCSC Ensembl
chr11:102471846..102472162hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181857
SamplesHG002
Known GenesMMP20
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3948185
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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