A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017682



Internal ID19106899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:50159790..50260292hg38UCSC Ensembl
Innerchr5:49455624..49556126hg19UCSC Ensembl
Innerchr5:49491381..49591883hg18UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg38100503
hg19100503
hg18100503
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5662n100
Supporting Variantsnssv3642094, nssv3642096, nssv3642093, nssv3642090, nssv3642091, nssv3642092, nssv3642095, nssv3642089
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)nsv1017682
Frequency
Sample Size11257
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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