A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109833



Internal ID21463760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:175698636..175705062hg38UCSC Ensembl
chr2:176563364..176569790hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg386427
hg196427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582464
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109833
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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