A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633780



Internal ID21582085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2386590..2386590hg38UCSC Ensembl
chr7:2426225..2426225hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155664, nssv17140539
SamplesHG00512, HG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633780
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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