A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860663



Internal ID22635598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49900244..49905539hg38UCSC Ensembl
chr13:50474380..50479675hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385296
hg195296
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n209
Supporting Variantsnssv17461168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860663
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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