A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739349



Internal ID20515322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:36485926..36486198hg38UCSC Ensembl
chr5:36486028..36486300hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38273
hg19273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739349
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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