A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405612



Internal ID21063165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78759787..78761157hg38UCSC Ensembl
chr5:78055610..78056980hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381371
hg191371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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