A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755992



Internal ID20531852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135985440..135985440hg38UCSC Ensembl
chr8:136997683..136997683hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755992
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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