A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613009



Internal ID16400418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:320856..322405hg38UCSC Ensembl
Innerchr9:320856..322405hg19UCSC Ensembl
Innerchr9:310856..312405hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381550
hg191550
hg181550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1125958, nssv1125947, nssv1125961, nssv1125965, nssv1125972, nssv1125948, nssv1125967, nssv1125959, nssv1125953, nssv1125966, nssv1125960, nssv1125949, nssv1125955, nssv1125954, nssv1125962, nssv1125957, nssv1125971, nssv1125952, nssv1125956, nssv1125951, nssv1125968, nssv1125963, nssv1125964, nssv1125950, nssv1125969, nssv1125970
Samples
Known GenesDOCK8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613009
Frequency
Sample Size17421
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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