A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847438



Internal ID22622373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9404663..9458818hg38UCSC Ensembl
chr7:9444293..9498448hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3854156
hg1954156
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847438
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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