A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405520



Internal ID21063073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78193834..78205010hg38UCSC Ensembl
chr5:77489658..77500834hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3811177
hg1911177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133950
Samples
Known GenesAP3B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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