A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015311



Internal ID19104528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12504379hg38UCSC Ensembl
Innerchr8:12260915..12361888hg19UCSC Ensembl
Innerchr8:12305286..12406259hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38100974
hg19100974
hg18100974
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7068n100
Supporting Variantsnssv3760125, nssv3760126, nssv3665836, nssv3665837, nssv3665838
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)nsv1015311
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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