A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633405



Internal ID21581710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141502241..141502241hg38UCSC Ensembl
chr7:141202041..141202041hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382496
hg192496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154875
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633405
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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