A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396356



Internal ID21053909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89873101..89874000hg38UCSC Ensembl
chr5:89168918..89169817hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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