A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966706



Internal ID19234022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1571570..1572570hg38UCSC Ensembl
Outerchr11:1592800..1593800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112601
Supporting Variants
SamplesKWS2
Known GenesDUSP8, MOB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966706
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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