A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939992



Internal ID22715394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39221221..39221270hg38UCSC Ensembl
chr13:39795358..39795407hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939992
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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