A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614826



Internal ID16402235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89058713..89059710hg38UCSC Ensembl
Innerchr9:91673628..91674625hg19UCSC Ensembl
Innerchr9:90863448..90864445hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139220
Samples
Known GenesSHC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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