A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576581



Internal ID21525021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13587088..13587168hg38UCSC Ensembl
chr6:13587320..13587400hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139786
SamplesHG02587
Known GenesSIRT5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576581
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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