A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862386



Internal ID22637321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129956290..129965544hg38UCSC Ensembl
chr7:129596130..129605384hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg389255
hg199255
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862386
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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