A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757365



Internal ID20533225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69956435..69956435hg38UCSC Ensembl
chr2:70183567..70183567hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757365
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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