A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043183



Internal ID19132402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80216401..80326098hg38UCSC Ensembl
Innerchr9:82831316..82941013hg19UCSC Ensembl
Innerchr9:82021136..82130833hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38109698
hg19109698
hg18109698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759779
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)nsv1043183
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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