A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3509907



Internal ID18808188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105345043..105539422hg38UCSC Ensembl
Innerchr10:107104801..107299180hg19UCSC Ensembl
Innerchr10:107094791..107289170hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38194380
hg19194380
hg18194380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043393
Supporting Variants
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)nssv3509907
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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