A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033954



Internal ID19123176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31570679..31604717hg38UCSC Ensembl
Innerchr9:31570677..31604715hg19UCSC Ensembl
Innerchr9:31560677..31594715hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3834039
hg1934039
hg1834039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7513n100
Supporting Variantsnssv3755930
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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