A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005800



Internal ID20572840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93023201..93026000hg38UCSC Ensembl
chr12:93416977..93419776hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471689
Supporting Variants
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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