A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145189



Internal ID15998375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130407868..130435428hg38UCSC Ensembl
Innerchr9:133283255..133310815hg19UCSC Ensembl
Innerchr9:132273076..132300636hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3827561
hg1927561
hg1827561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615522
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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