A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447097



Internal ID22113274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138650724..138650724hg38UCSC Ensembl
chr7:138335469..138335469hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762213
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447097
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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