A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582832



Internal ID21531349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11178598..11178712hg38UCSC Ensembl
chr8:11036107..11036221hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148706
SamplesNA19239
Known GenesXKR6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582832
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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