A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495779



Internal ID272875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81738424..82053192hg38UCSC Ensembl
chr11:81449466..81764234hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38314769
hg19314769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv84n206
Supporting Variantsnssv17048801
Samples
Known GenesMIR4300
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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