A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575605



Internal ID21524035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151090921..151090970hg38UCSC Ensembl
chr6:151412057..151412106hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146560
SamplesHG03065
Known GenesMTHFD1L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575605
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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