A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704190



Internal ID21376466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84080546..84080871hg38UCSC Ensembl
chr7:83709862..83710187hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388608
Supporting Variants
Samples
Known GenesSEMA3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704190
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.896552


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