A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127133



Internal ID18924322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:94012166..94012225hg38UCSC Ensembl
Outerchr10:95771923..95771982hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985491
SamplesKWS1
Known GenesPLCE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127133
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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