A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764104



Internal ID20539964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101925707..101925707hg38UCSC Ensembl
chr11:101796438..101796438hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265863
Samples
Known GenesKIAA1377
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764104
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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