A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350948



Internal ID21008501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:217407762..217420659hg38UCSC Ensembl
chr2:218272485..218285382hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3812898
hg1912898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085829
Samples
Known GenesDIRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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