A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755496



Internal ID20531356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141652128..141652128hg38UCSC Ensembl
chr5:141031695..141031695hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755496
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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