A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614852



Internal ID16402261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90024440..90338268hg38UCSC Ensembl
Innerchr9:92786722..93100550hg19UCSC Ensembl
Innerchr9:91826542..92140370hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38313829
hg19313829
hg18313829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139317
Samples
Known GenesLOC286370
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614852
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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