A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121846



Internal ID21480710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185222021..185222235hg38UCSC Ensembl
chr4:186143175..186143389hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576578
Supporting Variants
SamplesHG03683
Known GenesSNX25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121846
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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