A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016397



Internal ID19105616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12014484..12101436hg38UCSC Ensembl
Innerchr9:12014484..12101436hg19UCSC Ensembl
Innerchr9:12004484..12091436hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3886953
hg1986953
hg1886953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7445n100
Supporting Variantsnssv3690554
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)nsv1016397
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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