A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017027



Internal ID18759562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11575785..11799681hg38UCSC Ensembl
Innerchr9:11575785..11799681hg19UCSC Ensembl
Innerchr9:11565785..11789681hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38223897
hg19223897
hg18223897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689238
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)nsv1017027
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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