A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627678



Internal ID21575983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55210476..55210476hg38UCSC Ensembl
chr7:55278169..55278169hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154331
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627678
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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