A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580992



Internal ID21529488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75430774..75431315hg38UCSC Ensembl
chr7:75060055..75060595hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38542
hg19541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150868
SamplesHG01596
Known GenesPOM121C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580992
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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