A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756096



Internal ID20531956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178232830..178232830hg38UCSC Ensembl
chr5:177659831..177659831hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756096
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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