A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767823



Internal ID20543683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151090864..151090864hg38UCSC Ensembl
chr6:151412000..151412000hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286015
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767823
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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