A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393774



Internal ID21051327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74147946..74261374hg38UCSC Ensembl
chr4:75013663..75127091hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38113429
hg19113429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120954
Samples
Known GenesMTHFD2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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