A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985534



Internal ID19207437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:18808158..18808225hg38UCSC Ensembl
Outerchr11:18829705..18829772hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127166
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985534
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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