A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564703



Internal ID21513009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42327797..42328108hg38UCSC Ensembl
chr8:42185315..42185626hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143984
SamplesHG00731
Known GenesIKBKB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564703
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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