A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854863



Internal ID22629798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86549327..86551772hg38UCSC Ensembl
chr7:86178643..86181088hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382446
hg192446
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854863
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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