A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021623



Internal ID18764157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7368769..7941317hg38UCSC Ensembl
Innerchr8:7226291..7798839hg19UCSC Ensembl
Innerchr8:7213701..7836249hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38572549
hg19572549
hg18622549
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6910n100
Supporting Variantsnssv3678916, nssv3755016, nssv3755015, nssv3678914, nssv3755018, nssv3678912, nssv3755017, nssv3678911, nssv3678917, nssv3678915, nssv3678913
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, DEFB4B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021623
Frequency
Sample Size29084
Observed Gain7
Observed Loss4
Observed Complex0
Frequencyn/a


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