A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058434



Internal ID19147653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72776654..72817519hg38UCSC Ensembl
Innerchr17:70772793..70813658hg19UCSC Ensembl
Innerchr17:68284388..68325253hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3840866
hg1940866
hg1840866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3280n100
Supporting Variantsnssv3567771, nssv3567770, nssv3725154
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058434
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