A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917988



Internal ID22693209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139309263..139443484hg38UCSC Ensembl
chr8:140321507..140455727hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38134222
hg19134221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445236
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917988
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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