A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759125



Internal ID20534985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43308231..43308231hg38UCSC Ensembl
chr7:43347830..43347830hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273783
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759125
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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