A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110046



Internal ID18910600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:105469379..105469438hg38UCSC Ensembl
Outerchr9:108231660..108231719hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959280
SamplesKWS1
Known GenesFSD1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110046
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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