A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115837



Internal ID19284920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68233084..68245184hg38UCSC Ensembl
Outerchr9:70848000..70860100hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3812101
hg1912101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977646
SamplesKWS2
Known GenesCBWD3, CBWD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115837
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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