A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149553



Internal ID18855678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39107617..39115363hg38UCSC Ensembl
Outerchr9:65620499..65628200hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387747
hg197702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000858
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149553
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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