A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032463



Internal ID19121685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14038545..14109037hg38UCSC Ensembl
Innerchr8:13896054..13966546hg19UCSC Ensembl
Innerchr8:13940425..14010917hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3870493
hg1970493
hg1870493
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7101n100
Supporting Variantsnssv3675855
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)nsv1032463
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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