A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066483



Internal ID19155702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203166..6228490hg38UCSC Ensembl
Innerchr17:6106486..6131810hg19UCSC Ensembl
Innerchr17:6047210..6072534hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3825325
hg1925325
hg1825325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560147, nssv3560148
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)nsv1066483
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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