A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070022



Internal ID19317959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35620051..35620952hg38UCSC Ensembl
chr11:35641599..35642500hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768721
SamplesKWP1
Known GenesFJX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070022
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