A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630937



Internal ID21579242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20283695..20283695hg38UCSC Ensembl
chr7:20323318..20323318hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152277
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630937
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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