A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128729



Internal ID19260075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:101892697..101979797hg38UCSC Ensembl
Outerchr15:102432900..102520000hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3887101
hg1987101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1278n106
Supporting Variantsnssv3960642
SamplesKWS1
Known GenesDDX11L9, FAM138E, MIR6859-1, MIR6859-2, OR4F4, WASH3P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128729
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer