A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442071



Internal ID22108254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51357051..51357051hg38UCSC Ensembl
chr19:51860305..51860305hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767811
Samples
Known GenesETFB
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442071
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