A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861969



Internal ID22636904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10153153..10171814hg38UCSC Ensembl
chr8:10010663..10029324hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818662
hg1918662
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504302
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861969
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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