A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067521



Internal ID19156740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8941560..8967514hg38UCSC Ensembl
Innerchr19:9052236..9078190hg19UCSC Ensembl
Innerchr19:8913236..8939190hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3825955
hg1925955
hg1825955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564685
Samples
Known GenesMUC16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067521
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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