A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446764



Internal ID22112941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108911153..108911153hg38UCSC Ensembl
chr7:108551210..108551210hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765632
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446764
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer