A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128533



Internal ID18916609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131109637..131115537hg38UCSC Ensembl
Outerchr10:132907900..132913800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960432
SamplesKWS1
Known GenesTCERG1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128533
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer