A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003360



Internal ID19092579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:355495..452005hg38UCSC Ensembl
Innerchr4:349284..445794hg19UCSC Ensembl
Innerchr4:339284..435794hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3896511
hg1996511
hg1896511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5077n100
Supporting Variantsnssv3616091, nssv3616089, nssv3616090
Samples
Known GenesABCA11P, ZNF141, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003360
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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