A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134927



Internal ID19258776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:93122393..93122454hg38UCSC Ensembl
Outerchr9:95884675..95884736hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3988433
SamplesKWS1
Known GenesNINJ1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134927
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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