A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751088



Internal ID21384176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41657059..41657600hg38UCSC Ensembl
chr15:41949257..41949798hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38542
hg19542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432225
Supporting Variants
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751088
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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