A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142086



Internal ID18918827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1473941..1474070hg38UCSC Ensembl
Outerchr10:1516136..1516265hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993592
SamplesKWS2
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142086
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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