A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432535



Internal ID21394537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43651108..43651595hg38UCSC Ensembl
chr17:41728476..41728963hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15749822
SamplesMDQ045
Known GenesMEOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432535
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