A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448928



Internal ID22115106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96896864..96896864hg38UCSC Ensembl
chr5:96232568..96232568hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764493
Samples
Known GenesERAP2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448928
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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