A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032391



Internal ID18774925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150882981..150928922hg38UCSC Ensembl
Innerchr4:151804133..151850074hg19UCSC Ensembl
Innerchr4:152023583..152069524hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3845942
hg1945942
hg1845942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636080
Samples
Known GenesLRBA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032391
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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