A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3485470



Internal ID18726425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12054410..12123986hg38UCSC Ensembl
Innerchr10:12096409..12165985hg19UCSC Ensembl
Innerchr10:12136415..12205991hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3869577
hg1969577
hg1869577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036774
Supporting Variants
Samples
Known GenesDHTKD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3485470
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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