A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031526



Internal ID18774060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142158902..142226107hg38UCSC Ensembl
Innerchr8:143240263..143307468hg19UCSC Ensembl
Innerchr8:143238170..143305375hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3867206
hg1967206
hg1867206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7333n100
Supporting Variantsnssv3690088
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)nsv1031526
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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