A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003321



Internal ID19092540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18934428..19116202hg38UCSC Ensembl
Innerchr4:18936051..19117825hg19UCSC Ensembl
Innerchr4:18545149..18726923hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38181775
hg19181775
hg18181775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619871
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)nsv1003321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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