A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128307



Internal ID21505984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168588789..168588789hg38UCSC Ensembl
chr4:169509940..169509940hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625354
Supporting Variants
SamplesNA19983
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128307
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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