A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018564



Internal ID18761097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7357077..7513944hg38UCSC Ensembl
Innerchr8:7214599..7371466hg19UCSC Ensembl
Innerchr8:7202009..7358876hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38156868
hg19156868
hg18156868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6924n100
Supporting Variantsnssv3678518
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, SPAG11B, ZNF705G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018564
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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