A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129940



Internal ID21402681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165264185..165264185hg38UCSC Ensembl
chr4:166185337..166185337hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643854
Supporting Variants
SamplesHG00171
Known GenesKLHL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129940
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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