A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977985



Internal ID19240869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9964061..9964130hg38UCSC Ensembl
Outerchr11:9985608..9985677hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125180
Supporting Variants
SamplesKWS2
Known GenesSBF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977985
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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