A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849828



Internal ID22624763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76921..82060hg38UCSC Ensembl
chr10:122861..128000hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg385140
hg195140
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv137n209
Supporting Variantsnssv17459004, nssv17466286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849828
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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