A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982866



Internal ID19215083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64341843..64341923hg38UCSC Ensembl
Outerchr11:64109315..64109395hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119885
Supporting Variants
SamplesKWS1
Known GenesCCDC88B, MIR7155
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982866
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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