A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855798



Internal ID22630733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104204296..104206681hg38UCSC Ensembl
chr7:103844744..103847129hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg382386
hg192386
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500096, nssv17500095, nssv17500094
Samples
Known GenesORC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855798
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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