A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349718



Internal ID21007271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5125514..5154526hg38UCSC Ensembl
chr2:5265647..5294659hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3829013
hg1929013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349718
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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