A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432204



Internal ID21394206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31324798..31368797hg38UCSC Ensembl
chr15:31617001..31661000hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3844000
hg1944000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753829
SamplesSMI041
Known GenesKLF13
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432204
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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