A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125981



Internal ID19268203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:135610439..135610497hg38UCSC Ensembl
Outerchr9:138502285..138502343hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984190
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125981
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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