A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398668



Internal ID21056221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94058378..94067724hg38UCSC Ensembl
chr5:93394083..93403429hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg389347
hg199347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136418
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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