A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136228



Internal ID21497535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39101131..39101131hg38UCSC Ensembl
chr4:39102751..39102751hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619458
Supporting Variants
SamplesNA19238
Known GenesKLHL5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136228
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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