A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629477



Internal ID21577782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126635238..126635238hg38UCSC Ensembl
chr7:126275292..126275292hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg386732
hg196732
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154569
SamplesNA19239
Known GenesGRM8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629477
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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