A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629342



Internal ID21577647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21900387..21900387hg38UCSC Ensembl
chr7:21940005..21940005hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143806
SamplesHG00731
Known GenesDNAH11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629342
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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