A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043947



Internal ID19133166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123967180..123988125hg38UCSC Ensembl
Innerchr9:126729459..126750404hg19UCSC Ensembl
Innerchr9:125769280..125790225hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3820946
hg1920946
hg1820946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695228
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)nsv1043947
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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