A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009591



Internal ID19098809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68589559..68674295hg38UCSC Ensembl
Innerchr4:69455277..69540013hg19UCSC Ensembl
Innerchr4:69137872..69222608hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3884737
hg1984737
hg1884737
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5289n100
Supporting Variantsnssv3630223, nssv3630216, nssv3630217, nssv3630218, nssv3630222, nssv3630221, nssv3744084, nssv3630219, nssv3630220, nssv3630224
Samples
Known GenesUGT2B15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009591
Frequency
Sample Size11257
Observed Gain8
Observed Loss2
Observed Complex0
Frequencyn/a


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