A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614798



Internal ID16055521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88388083..88389167hg38UCSC Ensembl
Innerchr9:91002998..91004082hg19UCSC Ensembl
Innerchr9:90192818..90193902hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381085
hg191085
hg181085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139121
Samples
Known GenesSPIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614798
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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