A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849884



Internal ID22624819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73986589..73991951hg38UCSC Ensembl
chr8:74898824..74904186hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385363
hg195363
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509869
Samples
Known GenesLY96
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849884
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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