A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065953



Internal ID21467624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46867434..46867738hg38UCSC Ensembl
chr1:47333106..47333410hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569832
Supporting Variants
SamplesHG03065
Known GenesCYP4Z2P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065953
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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