A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469830



Internal ID21127383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90919063..90919477hg38UCSC Ensembl
chr12:91312840..91313254hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005558
Samples
Known GenesLINC00615
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469830
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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