A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032837



Internal ID18775371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20647170..20692439hg38UCSC Ensembl
Innerchr9:20647169..20692438hg19UCSC Ensembl
Innerchr9:20637169..20682438hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3845270
hg1945270
hg1845270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755832
Samples
Known GenesFOCAD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032837
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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