A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580155



Internal ID21528642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79536001..79536310hg38UCSC Ensembl
chr7:79165317..79165626hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151288
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580155
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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