A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022320



Internal ID19111538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8163549..8216832hg38UCSC Ensembl
Innerchr9:8163549..8216832hg19UCSC Ensembl
Innerchr9:8153549..8206832hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3853284
hg1953284
hg1853284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689120
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)nsv1022320
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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