A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034778



Internal ID19123999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21915873..21972691hg38UCSC Ensembl
Innerchr8:21773384..21830202hg19UCSC Ensembl
Innerchr8:21829330..21886148hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3856819
hg1956819
hg1856819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7131n100
Supporting Variantsnssv3685352, nssv3685351
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034778
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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