A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352392



Internal ID21009945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39013860..39014299hg38UCSC Ensembl
chr2:39241001..39241440hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086411
Samples
Known GenesSOS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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