A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354881



Internal ID22580550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96098958..96099904hg38UCSC Ensembl
chr11:95832122..95833068hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38947
hg19947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927241
Supporting Variants
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354881
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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