A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754568



Internal ID20530428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17577187..17577187hg38UCSC Ensembl
chr4:17578810..17578810hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754568
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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