A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970452



Internal ID19232555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:39547119..39547174hg38UCSC Ensembl
Outerchr11:39568669..39568724hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134107
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970452
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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