A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565267



Internal ID21513579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136541072..136545094hg38UCSC Ensembl
chr5:135876761..135880783hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384023
hg194023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133197
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565267
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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