A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050850



Internal ID19140069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9477948..9587658hg38UCSC Ensembl
Innerchr12:9630544..9740254hg19UCSC Ensembl
Innerchr12:9521811..9631521hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38109711
hg19109711
hg18109711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1373n100
Supporting Variantsnssv3517384
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)nsv1050850
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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