A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849211



Internal ID22624146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70568612..70581493hg38UCSC Ensembl
chr8:71480847..71493728hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3812882
hg1912882
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509780
Samples
Known GenesTRAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849211
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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