A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005722



Internal ID19094939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35374407..35409909hg38UCSC Ensembl
Innerchr4:35376029..35411531hg19UCSC Ensembl
Innerchr4:35052424..35087926hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3835503
hg1935503
hg1835503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5190n100
Supporting Variantsnssv3625007, nssv3625017, nssv3739343, nssv3625015, nssv3625008, nssv3625014, nssv3625010, nssv3741056, nssv3625021, nssv3625018, nssv3625016, nssv3739342, nssv3625011, nssv3741055, nssv3625012, nssv3625009, nssv3741054, nssv3625019, nssv3625013, nssv3741057, nssv3625020
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)nsv1005722
Frequency
Sample Size11257
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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