A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148289



Internal ID16001475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136093588..136157501hg38UCSC Ensembl
Innerchr9:138985434..139049347hg19UCSC Ensembl
Innerchr9:138125255..138189168hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3863914
hg1963914
hg1863914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615948
Supporting Variants
Samples
Known GenesC9orf69, NACC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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