A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107644



Internal ID21440825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:111836188..111836490hg38UCSC Ensembl
chr2:112593765..112594067hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573814
Supporting Variants
SamplesHG00732
Known GenesANAPC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107644
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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