A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350721



Internal ID21008274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27423075..27426242hg38UCSC Ensembl
chr2:27645942..27649109hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383168
hg193168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350721
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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