A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065970



Internal ID21434438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47179107..47179107hg38UCSC Ensembl
chr1:47644779..47644779hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618422
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065970
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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