A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043991



Internal ID19133210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:106371364..106421655hg38UCSC Ensembl
Innerchr9:109133645..109183936hg19UCSC Ensembl
Innerchr9:108173466..108223757hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3850292
hg1950292
hg1850292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697646
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)nsv1043991
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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