A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849983



Internal ID22624918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64577066..64579100hg38UCSC Ensembl
chr8:65489623..65491657hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382035
hg192035
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509673
Samples
Known GenesLOC401463
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849983
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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