A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110530



Internal ID19282446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40321082..40358882hg38UCSC Ensembl
Outerchr9:42466100..42503900hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3837801
hg1937801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960183
SamplesKWS1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110530
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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