A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067442



Internal ID19156661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70829343..70857856hg38UCSC Ensembl
Innerchr17:68825484..68853997hg19UCSC Ensembl
Innerchr17:66337079..66365592hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3828514
hg1928514
hg1828514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567763, nssv3567764, nssv3725153
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)nsv1067442
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer