A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866374



Internal ID22641309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137080402..137081874hg38UCSC Ensembl
chr7:136765149..136766621hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501338, nssv17503959
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866374
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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