A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112181



Internal ID21452654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237282692..237282692hg38UCSC Ensembl
chr2:238191335..238191335hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620255
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112181
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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