A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142091



Internal ID18901635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28863568..28863639hg38UCSC Ensembl
Outerchr10:29152497..29152568hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993595
SamplesKWS2
Known GenesC10orf126
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142091
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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