A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024712



Internal ID19113929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25540570..25552325hg38UCSC Ensembl
Innerchr8:25398086..25409841hg19UCSC Ensembl
Innerchr8:25454003..25465758hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811756
hg1911756
hg1811756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7149n100
Supporting Variantsnssv3685506
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024712
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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