A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111122



Internal ID21465702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213236803..213236939hg38UCSC Ensembl
chr2:214101527..214101663hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575846
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111122
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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