A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615941



Internal ID21564246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46377595..46377595hg38UCSC Ensembl
chr4:46379612..46379612hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132787
SamplesNA18939
Known GenesGABRA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615941
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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