A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443266



Internal ID22109449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33155705..33155705hg38UCSC Ensembl
chr7:33195317..33195317hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758832
Samples
Known GenesBBS9
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443266
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