A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005558



Internal ID20572599
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 StatusS
Merged Variantsnsv6469830
Supporting Variants
Samples
Known GenesLINC00615
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00129


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