A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755896



Internal ID19054177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28648389..28782315hg38UCSC Ensembl
Innerchr9:28648387..28782313hg19UCSC Ensembl
Innerchr9:28638387..28772313hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38133927
hg19133927
hg18133927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026302
Supporting Variants
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3755896
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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