A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856908



Internal ID22631843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39142892..39144091hg38UCSC Ensembl
chr8:39000411..39001610hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509195, nssv17506060
Samples
Known GenesADAM32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856908
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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