A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067070



Internal ID21478335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87359226..87359226hg38UCSC Ensembl
chr1:87824909..87824909hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613998
Supporting Variants
SamplesHG03486
Known GenesLOC100505768
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067070
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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