A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045322



Internal ID19134541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84052078..84086997hg38UCSC Ensembl
Innerchr9:86666993..86701912hg19UCSC Ensembl
Innerchr9:85856813..85891732hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3834920
hg1934920
hg1834920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697525, nssv3759781, nssv3697526
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)nsv1045322
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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