A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031236



Internal ID18773769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187526594..189035370hg38UCSC Ensembl
Innerchr4:188447748..189956524hg19UCSC Ensembl
Innerchr4:188684742..190193518hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381508777
hg191508777
hg181508777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744536
Samples
Known GenesLINC01060, TRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031236
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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