A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061805



Internal ID21512273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169811765..169811765hg38UCSC Ensembl
chr1:169780906..169780906hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609223
Supporting Variants
SamplesNA24385
Known GenesC1orf112
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061805
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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