A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018846



Internal ID19108063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12513862hg38UCSC Ensembl
Innerchr8:12260915..12371371hg19UCSC Ensembl
Innerchr8:12305286..12415742hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38110457
hg19110457
hg18110457
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7068n100
Supporting Variantsnssv3665894, nssv3665895, nssv3665887, nssv3760132, nssv3665899, nssv3665892, nssv3665889, nssv3665888, nssv3665897, nssv3665896, nssv3665893, nssv3665891, nssv3760130, nssv3665898, nssv3665886, nssv3665890, nssv3760131
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018846
Frequency
Sample Size11257
Observed Gain4
Observed Loss13
Observed Complex0
Frequencyn/a


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