A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024706



Internal ID18767238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7364449..7886530hg38UCSC Ensembl
Innerchr8:7221971..7744052hg19UCSC Ensembl
Innerchr8:7209381..7781462hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38522082
hg19522082
hg18572082
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6909n100
Supporting Variantsnssv3678849, nssv3678850
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024706
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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