A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129490



Internal ID18931406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14568367..14568420hg38UCSC Ensembl
Outerchr10:14610366..14610419hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962951
SamplesKWS1
Known GenesFAM107B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129490
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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