A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069841



Internal ID19326775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24834959..24835061hg38UCSC Ensembl
chr15:25080106..25080208hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762171
SamplesKWP1
Known GenesSNRPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069841
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