A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109931



Internal ID21425127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195568372..195568372hg38UCSC Ensembl
chr2:196433096..196433096hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610458
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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