A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033098



Internal ID19122320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49960733..50053132hg38UCSC Ensembl
Innerchr8:50873293..50965692hg19UCSC Ensembl
Innerchr8:51035846..51128245hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3892400
hg1992400
hg1892400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687470
Samples
Known GenesSNTG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033098
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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