A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111122



Internal ID19253216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3605676..3605756hg38UCSC Ensembl
Outerchr16:3655677..3655757hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962347
SamplesKWS1
Known GenesSLX4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111122
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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