A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577428



Internal ID21525881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73540646..73540963hg38UCSC Ensembl
chr7:72954976..72955293hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140794
SamplesHG03486
Known GenesBCL7B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577428
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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