A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572749



Internal ID21521142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94658832..94658945hg38UCSC Ensembl
chr5:93994537..93994650hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154456
SamplesHG03486
Known GenesANKRD32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572749
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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