A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760361



Internal ID20536221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178157170..178157170hg38UCSC Ensembl
chr5:177584171..177584171hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276726
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760361
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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