A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354443



Internal ID21011996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46907100..46910851hg38UCSC Ensembl
chr2:47134239..47137990hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg383752
hg193752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089368
Samples
Known GenesMCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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