A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021182



Internal ID19110400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170909409..171003551hg38UCSC Ensembl
Innerchr4:171830560..171924702hg19UCSC Ensembl
Innerchr4:172067135..172161277hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3894143
hg1994143
hg1894143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5470n100
Supporting Variantsnssv3635393
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021182
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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