A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026123



Internal ID19115340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28588577..28761733hg38UCSC Ensembl
Innerchr9:28588575..28761731hg19UCSC Ensembl
Innerchr9:28578575..28751731hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38173157
hg19173157
hg18173157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7491n100
Supporting Variantsnssv3692050, nssv3692054, nssv3692049, nssv3692051, nssv3755888, nssv3692053, nssv3692052, nssv3692047, nssv3692048, nssv3755887, nssv3755889, nssv3755886
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)nsv1026123
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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