A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081148



Internal ID21990381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2312032..2312032hg38UCSC Ensembl
chr11:2333262..2333262hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578224
Samples
Known GenesTSPAN32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081148
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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