A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846266



Internal ID22621201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22561194..22571008hg38UCSC Ensembl
chr7:22600813..22610627hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg389815
hg199815
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504762
Samples
Known GenesLOC100506178
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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