A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447359



Internal ID22113536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156120652..156120652hg38UCSC Ensembl
chr7:155913346..155913346hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762303
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447359
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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