A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352448



Internal ID22578117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85631433..85631487hg38UCSC Ensembl
chr11:85342477..85342531hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926167
Supporting Variants
Samples
Known GenesTMEM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352448
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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