A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141612



Internal ID19281189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42662297..42670897hg38UCSC Ensembl
Outerchr9:44339100..44347700hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388601
hg198601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4010n106
Supporting Variantsnssv3993117
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141612
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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