A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737589



Internal ID20513551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26636073..26636135hg38UCSC Ensembl
chr13:27210210..27210272hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266410
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737589
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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