A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690729



Internal ID18989010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22740233..22778493hg38UCSC Ensembl
Innerchr9:22740232..22778492hg19UCSC Ensembl
Innerchr9:22730232..22768492hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3838261
hg1938261
hg1838261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020027
Supporting Variants
Samples
Known GenesFLJ35282
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690729
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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