A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012409



Internal ID19101626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:355495..429034hg38UCSC Ensembl
Innerchr4:349284..422823hg19UCSC Ensembl
Innerchr4:339284..412823hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3873540
hg1973540
hg1873540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5077n100
Supporting Variantsnssv3616088
Samples
Known GenesABCA11P, ZNF141
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012409
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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