A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045811



Internal ID19135030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:119450086..119662490hg38UCSC Ensembl
Innerchr9:122212364..122424768hg19UCSC Ensembl
Innerchr9:121252185..121464589hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38212405
hg19212405
hg18212405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759821
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)nsv1045811
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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