A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141458



Internal ID20708498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30872231..30891707hg38UCSC Ensembl
chr6:30840008..30859484hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3819477
hg1919477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403437
Supporting Variants
Samples
Known GenesDDR1, MIR4640
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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