A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111514



Internal ID21507417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230841280..230842232hg38UCSC Ensembl
chr2:231705995..231706947hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570077
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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