A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576326



Internal ID21524764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139950797..139950892hg38UCSC Ensembl
chr7:139650596..139650691hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142098
SamplesNA19238
Known GenesTBXAS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576326
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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