A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385571



Internal ID21043124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14818440..14819664hg38UCSC Ensembl
chr5:14818549..14819773hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381225
hg191225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125914
Samples
Known GenesANKH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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