A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627704



Internal ID21576009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143252778..143252778hg38UCSC Ensembl
chr8:144334948..144334948hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382288
hg192288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147541
SamplesHG01596
Known GenesZFP41
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627704
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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