A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406297



Internal ID21063850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147869867..147874176hg38UCSC Ensembl
chr5:147249430..147253739hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg384310
hg194310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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