A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750782



Internal ID20526642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66431852..66431852hg38UCSC Ensembl
chr2:66658984..66658984hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278704
Samples
Known GenesMEIS1-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750782
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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