A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570823



Internal ID21519193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78085826..78085893hg38UCSC Ensembl
chr7:77715143..77715210hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152196
SamplesNA19239
Known GenesMAGI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570823
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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