A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404369



Internal ID21061922
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 StatusM
Merged Variants
Supporting Variantsnssv18148046
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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