A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125874



Internal ID18928917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:39905999..39906091hg38UCSC Ensembl
Outerchr6:39873775..39873867hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984080
SamplesKWS2
Known GenesMOCS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125874
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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