A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405509



Internal ID21063062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:93757101..93767200hg38UCSC Ensembl
chr5:93092807..93102906hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215020
Samples
Known GenesFAM172A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405509
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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