A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751676



Internal ID20527536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185908298..185908298hg38UCSC Ensembl
chr4:186829452..186829452hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273851
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751676
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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