A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016978



Internal ID18759513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21171268..21214878hg38UCSC Ensembl
Innerchr9:21171267..21214877hg19UCSC Ensembl
Innerchr9:21161267..21204877hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3843611
hg1943611
hg1843611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7474n100
Supporting Variantsnssv3690706
Samples
Known GenesIFNA10, 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)nsv1016978
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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