A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564954



Internal ID21513262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85314271..85316321hg38UCSC Ensembl
chr7:84943587..84945637hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382051
hg192051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150510
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564954
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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