A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996108



Internal ID19194324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:127260335..127262136hg38UCSC Ensembl
Outerchr10:129058599..129060400hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150633
Supporting Variants
SamplesKWB1
Known GenesDOCK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996108
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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