A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746625



Internal ID20522639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46316384..46322790hg38UCSC Ensembl
chr7:46355982..46362388hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg386407
hg196407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746625
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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