A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015607



Internal ID19104824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28957530..29119537hg38UCSC Ensembl
Innerchr9:28957528..29119535hg19UCSC Ensembl
Innerchr9:28947528..29109535hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38162008
hg19162008
hg18162008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755902
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)nsv1015607
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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