A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903868



Internal ID22679040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150996209..151015374hg38UCSC Ensembl
chr6:151317345..151336510hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3819166
hg1919166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413028
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903868
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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