A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989168



Internal ID18871040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132213741..132214033hg38UCSC Ensembl
Outerchr11:132083635..132083927hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135604
Supporting Variants
SamplesKWS1
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989168
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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