A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964968



Internal ID18863288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12130997..12131321hg38UCSC Ensembl
Outerchr11:12152544..12152868hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135428
Supporting Variants
SamplesKWS1
Known GenesMICAL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964968
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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