A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026829



Internal ID18769360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12024338..12513862hg38UCSC Ensembl
Innerchr8:11881847..12371371hg19UCSC Ensembl
Innerchr8:11919256..12415742hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38489525
hg19489525
hg18496487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7015n100
Supporting Variantsnssv3681745
Samples
Known GenesDEFB109P1, DEFB130, FAM66A, FAM66D, FAM86B1, FAM86B2, FAM90A25P, FAM90A2P, LOC100133267, LOC100506990, LOC392196, LOC649352, USP17L2, USP17L7, ZNF705D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026829
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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