A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405313



Internal ID21062866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89968838..90067279hg38UCSC Ensembl
chr5:89264655..89363096hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3898442
hg1998442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134290
Samples
Known GenesMIR3660
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405313
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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