A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007862



Internal ID19097081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68569694..68674295hg38UCSC Ensembl
Innerchr4:69435412..69540013hg19UCSC Ensembl
Innerchr4:69118007..69222608hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38104602
hg19104602
hg18104602
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5278n100
Supporting Variantsnssv3628890, nssv3628884, nssv3628887, nssv3628877, nssv3628891, nssv3628885, nssv3628881, nssv3628889, nssv3743957, nssv3628883, nssv3628880, nssv3628876, nssv3628878, nssv3628886, nssv3628882, nssv3628893, nssv3743956, nssv3628879, nssv3628888, nssv3628892
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)nsv1007862
Frequency
Sample Size11257
Observed Gain19
Observed Loss1
Observed Complex0
Frequencyn/a


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