A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353351



Internal ID21010904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27109188..27112149hg38UCSC Ensembl
chr2:27332056..27335017hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382962
hg192962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085688
Samples
Known GenesCGREF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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