A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154456



Internal ID21477997
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 StatusS
Merged Variantsnsv5572749
Supporting Variants
SamplesHG03486
Known GenesANKRD32
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154456
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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