A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017199



Internal ID18759734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142158902..142225742hg38UCSC Ensembl
Innerchr8:143240263..143307103hg19UCSC Ensembl
Innerchr8:143238170..143305010hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3866841
hg1966841
hg1866841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7333n100
Supporting Variantsnssv3690087
Samples
Known GenesLINC00051, MIR4472-1, TSNARE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017199
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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