A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129498



Internal ID19286252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:95447028..95448263hg38UCSC Ensembl
Outerchr10:97206785..97208020hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3963730
SamplesKWS1
Known GenesSORBS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129498
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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