A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131807



Internal ID21479538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:85506540..85506665hg38UCSC Ensembl
chr4:86427693..86427818hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583708
Supporting Variants
SamplesHG03486
Known GenesARHGAP24
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131807
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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