A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150753



Internal ID18850969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63780365..63844266hg38UCSC Ensembl
Outerchr9:68376099..68440000hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3863902
hg1963902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996229
SamplesKWB1
Known GenesLOC642236
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150753
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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