A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032482



Internal ID18775016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7172456..7542794hg38UCSC Ensembl
Innerchr8:7029978..7400316hg19UCSC Ensembl
Innerchr8:7017388..7387726hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38370339
hg19370339
hg18370339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6898n100
Supporting Variantsnssv3677647
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4B, FAM66B, LINC00965, PRR23D1, PRR23D2, SPAG11B, USP17L1P, USP17L4, ZNF705G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032482
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer