A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139979



Internal ID19286617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63316828..63344528hg38UCSC Ensembl
Outerchr9:67271800..67299500hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3827701
hg1927701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978315
SamplesKWS2
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139979
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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