A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408101



Internal ID21065654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83063886..83064502hg38UCSC Ensembl
chr5:82359705..82360321hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133021
Samples
Known GenesSCARNA18, TMEM167A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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