A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021373



Internal ID19110590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28190071..28347681hg38UCSC Ensembl
Innerchr9:28190069..28347679hg19UCSC Ensembl
Innerchr9:28180069..28337679hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38157611
hg19157611
hg18157611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7490n100
Supporting Variantsnssv3692025, nssv3692028, nssv3692027, nssv3692026, nssv3692030, nssv3755881, nssv3755882, nssv3755883, nssv3692029
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)nsv1021373
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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