A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618170



Internal ID21566475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182772265..182772265hg38UCSC Ensembl
chr2:183636992..183636992hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110630
SamplesHG03009
Known GenesDNAJC10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618170
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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