A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021067



Internal ID18763601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:158051130..158254323hg38UCSC Ensembl
Innerchr4:158972282..159175475hg19UCSC Ensembl
Innerchr4:159191732..159394925hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38203194
hg19203194
hg18203194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636157
Samples
Known GenesFAM198B, TMEM144
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021067
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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