A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857098



Internal ID22632033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135148751..135149950hg38UCSC Ensembl
chr7:134833503..134834702hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501317, nssv17501318
Samples
Known GenesTMEM140
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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