A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767638



Internal ID20543498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114306310..114306310hg38UCSC Ensembl
chr10:116066069..116066069hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273193
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767638
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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