A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033392



Internal ID19122614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14643653..14657695hg38UCSC Ensembl
Innerchr9:14643651..14657693hg19UCSC Ensembl
Innerchr9:14633651..14647693hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3814043
hg1914043
hg1814043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690619
Samples
Known GenesZDHHC21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033392
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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