A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060994



Internal ID21486663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159042587..159046746hg38UCSC Ensembl
chr1:159012377..159016536hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5577818
Supporting Variants
SamplesNA12878
Known GenesIFI16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060994
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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