A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022112



Internal ID18764646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187530002..188139456hg38UCSC Ensembl
Innerchr4:188451156..189060610hg19UCSC Ensembl
Innerchr4:188688150..189297604hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38609455
hg19609455
hg18609455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5499n100
Supporting Variantsnssv3635659, nssv3635660
Samples
Known GenesTRIML1, 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)nsv1022112
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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