A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270053



Internal ID20479271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68929844..68929844hg38UCSC Ensembl
chr11:68697312..68697312hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753778
Supporting Variants
Samples
Known GenesIGHMBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270053
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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