A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403008



Internal ID21060561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88254969..88265466hg38UCSC Ensembl
chr5:87550786..87561283hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3810498
hg1910498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134812
Samples
Known GenesTMEM161B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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