A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026110



Internal ID18768642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143318672..143370995hg38UCSC Ensembl
Innerchr4:144239825..144292148hg19UCSC Ensembl
Innerchr4:144459275..144511598hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3852324
hg1952324
hg1852324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744247
Samples
Known GenesGAB1, MIR3139
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026110
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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