A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967297



Internal ID19228041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:9103167..9109167hg38UCSC Ensembl
Outerchr21:9942000..9948000hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112797
Supporting Variants
SamplesKWS2
Known GenesTEKT4P2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967297
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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