A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847380



Internal ID22622315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:60988528..60997404hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388877
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500565, nssv17500566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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