A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069821



Internal ID19318312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102509462..102509963hg38UCSC Ensembl
chr14:102975799..102976300hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768399
SamplesKWP1
Known GenesANKRD9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069821
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