A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018864



Internal ID18761397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27195842..27294817hg38UCSC Ensembl
Innerchr9:27195840..27294815hg19UCSC Ensembl
Innerchr9:27185840..27284815hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3898976
hg1998976
hg1898976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692012, nssv3692010, nssv3692011
Samples
Known GenesEQTN, LINC00032, TEK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018864
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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