A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352490



Internal ID21010043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98667025..98669212hg38UCSC Ensembl
chr2:99283488..99285675hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090486
Samples
Known GenesMGAT4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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