A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110179



Internal ID18917051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:79704044..79711544hg38UCSC Ensembl
Outerchr10:81463800..81471300hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387501
hg197501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959446
SamplesKWS1
Known GenesNUTM2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110179
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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