A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443742



Internal ID22109923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44992569..44992569hg38UCSC Ensembl
chr7:45032168..45032168hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757992
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443742
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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