A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018561



Internal ID18761094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21181455..21228249hg38UCSC Ensembl
Innerchr9:21181454..21228248hg19UCSC Ensembl
Innerchr9:21171454..21218248hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3846795
hg1946795
hg1846795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7474n100
Supporting Variantsnssv3690708, nssv3690709, nssv3690710
Samples
Known GenesIFNA10, IFNA16, IFNA17, IFNA4, IFNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018561
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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