A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377092



Internal ID21034645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152554015..152671746hg38UCSC Ensembl
chr4:153475167..153592898hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38117732
hg19117732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112028
Samples
Known GenesTMEM154
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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