A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073536



Internal ID19317378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11228570..11228623hg38UCSC Ensembl
chr6:11228803..11228856hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768684
SamplesKWP1
Known GenesNEDD9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073536
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