A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068246



Internal ID21461610
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 StatusS
Merged Variantsnsv5573273
Supporting Variants
SamplesHG02818
Known GenesSLC2A5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068246
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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