A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354151



Internal ID21011704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:148236673..148263457hg38UCSC Ensembl
chr2:148994242..149021026hg19UCSC Ensembl
Cytoband2q23.1
Allele length
AssemblyAllele length
hg3826785
hg1926785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079364
Samples
Known GenesMBD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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