A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410973



Internal ID21068526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152346956..152351149hg38UCSC Ensembl
chr5:151726517..151730710hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg384194
hg194194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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