A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611342



Internal ID20984413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151060879..151065906hg38UCSC Ensembl
chr6:151382015..151387042hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385028
hg195028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141062
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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