A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615027



Internal ID16055750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102284644..103457001hg38UCSC Ensembl
Innerchr9:105046926..106219283hg19UCSC Ensembl
Innerchr9:104086747..105259104hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381172358
hg191172358
hg181172358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140607
Samples
Known GenesCYLC2, LINC00587
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615027
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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