A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119314



Internal ID19270209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68305584..68329584hg38UCSC Ensembl
Outerchr9:70920500..70944500hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3824001
hg1924001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959752
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119314
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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