A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016276



Internal ID18758811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19517487..19577636hg38UCSC Ensembl
Innerchr8:19374998..19435147hg19UCSC Ensembl
Innerchr8:19419278..19479427hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3860150
hg1960150
hg1860150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7130n100
Supporting Variantsnssv3684218
Samples
Known GenesCSGALNACT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016276
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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