A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970435



Internal ID18898734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12922185..12922462hg38UCSC Ensembl
Outerchr11:12943732..12944009hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134093
Supporting Variants
SamplesKWS2
Known GenesTEAD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970435
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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