A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432253



Internal ID21394255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71182072..71185597hg38UCSC Ensembl
chr15:71474411..71477936hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383526
hg193526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262n172
Supporting Variantsnssv15751555
SamplesMDQ010
Known GenesTHSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432253
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