A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762888



Internal ID20538748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19832902..19832902hg38UCSC Ensembl
chr13:20407042..20407042hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264224
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762888
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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