A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354106



Internal ID21011659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72679239..72687548hg38UCSC Ensembl
chr2:72906368..72914677hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg388310
hg198310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089684
Samples
Known GenesEXOC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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