A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606655



Internal ID20979726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151062375..151072267hg38UCSC Ensembl
chr6:151383511..151393403hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg389893
hg199893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141063
Samples
Known GenesMTHFD1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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