A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139404



Internal ID20706444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13392014..13399108hg38UCSC Ensembl
chr6:13392246..13399340hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg387095
hg197095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411428
Supporting Variants
Samples
Known GenesGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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