A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18148046



Internal ID20715086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88626289..88634470hg38UCSC Ensembl
chr6:89336008..89344189hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg388182
hg198182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404369
Supporting Variants
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18148046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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