A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736940



Internal ID20512894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132275299..132275359hg38UCSC Ensembl
chr5:131610992..131611052hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736940
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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