A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020971



Internal ID19110189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123927331..123961439hg38UCSC Ensembl
Innerchr8:124939571..124973679hg19UCSC Ensembl
Innerchr8:125008752..125042860hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3834109
hg1934109
hg1834109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691501
Samples
Known GenesFER1L6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020971
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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