A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934929



Internal ID22710262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26510483..26511094hg38UCSC Ensembl
chr13:27084620..27085231hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934929
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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