A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020893



Internal ID18763427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12025123..12349015hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg18323893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7020n100
Supporting Variantsnssv3681826
Samples
Known GenesDEFB109P1, DEFB130, FAM66A, FAM66D, FAM86B1, FAM86B2, FAM90A25P, FAM90A2P, LOC100133267, LOC100506990, LOC649352, USP17L2, USP17L7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020893
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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