A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753619



Internal ID20529479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96378182..96378182hg38UCSC Ensembl
chr7:96007494..96007494hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753619
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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