A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629052



Internal ID21577357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154545497..154545497hg38UCSC Ensembl
chr7:154242582..154242582hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140922
SamplesHG03486
Known GenesDPP6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629052
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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