A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440065



Internal ID22106242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38123801..38123879hg38UCSC Ensembl
chr19:38614441..38614519hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756938
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440065
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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