A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153561



Internal ID19195542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63277827..63344228hg38UCSC Ensembl
Outerchr9:67232799..67299200hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3866402
hg1966402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002216
SamplesKWB1
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153561
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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