A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17064391



Internal ID21452681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27293833..27293833hg38UCSC Ensembl
chr1:27620324..27620324hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383331
hg193331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612733
Supporting Variants
SamplesHG01596
Known GenesWDTC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17064391
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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