A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132711



Internal ID18933722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39092424..39097600hg38UCSC Ensembl
Outerchr9:65638200..65643400hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg385177
hg195201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987501
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132711
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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