A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112603



Internal ID21458598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240318574..240318759hg38UCSC Ensembl
chr2:241257991..241258176hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574553
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112603
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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