A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149592



Internal ID19195098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:66178621..66183622hg38UCSC Ensembl
Outerchr9:43159199..43164200hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000897
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149592
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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