A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132714



Internal ID19276198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63038928..63052128hg38UCSC Ensembl
Outerchr9:66943900..66957100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3813201
hg1913201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987504
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132714
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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