A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335850



Internal ID20993403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6732971..6733361hg38UCSC Ensembl
chr2:6873102..6873492hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089533
Samples
Known GenesLINC00487
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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