A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757527



Internal ID20533387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202577529..202577529hg38UCSC Ensembl
chr2:203442252..203442252hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757527
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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