A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050112



Internal ID19139331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:116735220..116766649hg38UCSC Ensembl
Innerchr9:119497499..119528928hg19UCSC Ensembl
Innerchr9:118537320..118568749hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3831430
hg1931430
hg1831430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695172
Samples
Known GenesASTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050112
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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