A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074844



Internal ID18973297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17277055..17277304hg38UCSC Ensembl
chr9:17277053..17277302hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38250
hg19250
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769966
SamplesKWP1
Known GenesCNTLN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074844
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