A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079566



Internal ID21510789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25590144..25590144hg38UCSC Ensembl
chr12:25743078..25743078hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661761
Supporting Variants
SamplesNA24385
Known GenesIFLTD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079566
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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