A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139417



Internal ID20706457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13421997..13427957hg38UCSC Ensembl
chr6:13422229..13428189hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385961
hg195961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415040
Supporting Variants
Samples
Known GenesGFOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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