A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372902



Internal ID21030455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95664001..95665400hg38UCSC Ensembl
chr3:95382845..95384244hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104053
Samples
Known GenesMTHFD2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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