A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921807



Internal ID22697031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34577349..34582726hg38UCSC Ensembl
chr8:34434867..34440244hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385378
hg195378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921807
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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