A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122559



Internal ID19267211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113781190..113781275hg38UCSC Ensembl
Outerchr10:115540949..115541034hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970770
SamplesKWS2
Known GenesPLEKHS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122559
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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