A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571029



Internal ID21519402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28961157..28961415hg38UCSC Ensembl
chr7:29000773..29001031hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140071
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571029
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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