A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847376



Internal ID22622311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:60950108..60955144hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385037
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500554, nssv17508312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847376
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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