A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067177



Internal ID21482121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95522169..95522169hg38UCSC Ensembl
chr1:95987725..95987725hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg386136
hg196136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608943
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067177
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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