A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017771



Internal ID19106988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167886977..168072721hg38UCSC Ensembl
Innerchr4:168808128..168993872hg19UCSC Ensembl
Innerchr4:169044703..169230447hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38185745
hg19185745
hg18185745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5464n100
Supporting Variantsnssv3635319
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)nsv1017771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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