A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446235



Internal ID22112414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894052..39894052hg38UCSC Ensembl
chr15:40186253..40186253hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759174
Samples
Known GenesGPR176
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446235
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