A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396799



Internal ID21054352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55964401..55965500hg38UCSC Ensembl
chr5:55260229..55261328hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131777
Samples
Known GenesIL6ST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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