A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110812



Internal ID21424722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186572387..186572568hg38UCSC Ensembl
chr2:187437114..187437295hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581717
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110812
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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