A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847578



Internal ID22622513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77571..83220hg38UCSC Ensembl
chr10:123511..129160hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg385650
hg195650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv137n209
Supporting Variantsnssv17463370, nssv17465874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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