A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019053



Internal ID19108270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14336731..14429043hg38UCSC Ensembl
Innerchr8:14194240..14286552hg19UCSC Ensembl
Innerchr8:14238611..14330923hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3892313
hg1992313
hg1892313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7104n100
Supporting Variantsnssv3675866
Samples
Known GenesSGCZ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019053
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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