A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945574



Internal ID22721053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:64951517..64956250hg38UCSC Ensembl
chr13:65525649..65530382hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945574
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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