A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573273



Internal ID21521675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9063674..9063993hg38UCSC Ensembl
chr1:9123733..9124052hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068246
SamplesHG02818
Known GenesSLC2A5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573273
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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