A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158938



Internal ID21488740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75927807..75927807hg38UCSC Ensembl
chr6:76637524..76637524hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg384784
hg194784
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640213
Supporting Variants
SamplesNA18939
Known GenesIMPG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158938
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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