A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636593



Internal ID21584898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155973770..155973770hg38UCSC Ensembl
chr7:155766464..155766464hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159358
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636593
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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