A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016983



Internal ID19106200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22412949..22672063hg38UCSC Ensembl
Innerchr9:22412948..22672062hg19UCSC Ensembl
Innerchr9:22402948..22662062hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38259115
hg19259115
hg18259115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690725
Samples
Known GenesDMRTA1, FLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016983
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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