A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761335



Internal ID20537195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159980218..159980218hg38UCSC Ensembl
chr6:160401250..160401250hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293358
Samples
Known GenesIGF2R
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761335
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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