A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415254



Internal ID21072807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128940654..128970813hg38UCSC Ensembl
chr5:128276347..128306506hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3830160
hg1930160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124438
Samples
Known GenesSLC27A6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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