A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963604



Internal ID18889809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:12131046..12131317hg38UCSC Ensembl
Outerchr11:12152593..12152864hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111470
Supporting Variants
SamplesKWS2
Known GenesMICAL2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963604
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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