A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898092



Internal ID22673203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138510194..138510448hg38UCSC Ensembl
chr5:137845883..137846137hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413396
Samples
Known GenesETF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898092
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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