A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741367



Internal ID20517344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94658945..94659056hg38UCSC Ensembl
chr5:93994650..93994761hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261007
Samples
Known GenesANKRD32
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741367
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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