A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034783



Internal ID19124004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12008565..12110043hg38UCSC Ensembl
Innerchr9:12008565..12110043hg19UCSC Ensembl
Innerchr9:11998565..12100043hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38101479
hg19101479
hg18101479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7445n100
Supporting Variantsnssv3690553
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)nsv1034783
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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