A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749800



Internal ID20525834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60581607..60581704hg38UCSC Ensembl
chr13:61155741..61155838hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749800
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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