A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126992



Internal ID21459386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168793123..168793123hg38UCSC Ensembl
chr4:169714274..169714274hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644210
Supporting Variants
SamplesHG02818
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126992
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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