A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115797



Internal ID18920308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:11100..39200hg38UCSC Ensembl
Outerchr9:11100..39200hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3828101
hg1928101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3939n106
Supporting Variantsnssv3977606
SamplesKWS2
Known GenesDDX11L5, FAM138C, WASH1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115797
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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