A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581573



Internal ID21530074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155886340..155886407hg38UCSC Ensembl
chr7:155679034..155679101hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159566
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581573
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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