A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125032



Internal ID19254855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64455214..64471035hg38UCSC Ensembl
Outerchr9:43025900..43041700hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3815822
hg1915801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4004n106
Supporting Variantsnssv3977837
SamplesKWS2
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125032
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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