A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760779



Internal ID20536639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26973618..26973618hg38UCSC Ensembl
chr2:27196486..27196486hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286685
Samples
Known GenesMAPRE3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760779
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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