A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122300



Internal ID21419533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39408925..39408925hg38UCSC Ensembl
chr4:39410545..39410545hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620028
Supporting Variants
SamplesHG00731
Known GenesKLB, MIR1273H
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122300
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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