A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624616



Internal ID21572921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44992613..44992613hg38UCSC Ensembl
chr7:45032212..45032212hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150019
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624616
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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