A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511679



Internal ID288251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81793600..81821000hg38UCSC Ensembl
chr13:82367735..82395135hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3827401
hg1927401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511679
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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