A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016226



Internal ID19105445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15841109..15875323hg38UCSC Ensembl
Innerchr9:15841107..15875321hg19UCSC Ensembl
Innerchr9:15831107..15865321hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3834215
hg1934215
hg1834215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7461n100
Supporting Variantsnssv3690630, nssv3690628, nssv3690629
Samples
Known GenesCCDC171
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016226
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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