A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759951



Internal ID20535811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85277441..85277441hg38UCSC Ensembl
chr1:85743124..85743124hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261380
Samples
Known GenesLOC646626
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759951
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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