A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119272



Internal ID19272464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:65246747..65254047hg38UCSC Ensembl
Outerchr9:42748500..42755800hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg387301
hg197301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4003n106
Supporting Variantsnssv3959709
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119272
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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