A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443744



Internal ID22109925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47362697..47362697hg38UCSC Ensembl
chr7:47402295..47402295hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767108
Samples
Known GenesTNS3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443744
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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