A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067361



Internal ID21480209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:96398098..96422410hg38UCSC Ensembl
chr1:96863654..96887966hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3824313
hg1924313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577502
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067361
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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