A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028530



Internal ID19117748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167887449..168072721hg38UCSC Ensembl
Innerchr4:168808600..168993872hg19UCSC Ensembl
Innerchr4:169045175..169230447hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38185273
hg19185273
hg18185273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5464n100
Supporting Variantsnssv3744507, nssv3635326
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)nsv1028530
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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