A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447178



Internal ID22113355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3085812..3085812hg38UCSC Ensembl
chr10:3128004..3128004hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762387
Samples
Known GenesPFKP
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447178
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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