A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044870



Internal ID19134089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6351298..6377500hg38UCSC Ensembl
Innerchr10:6393260..6419462hg19UCSC Ensembl
Innerchr10:6433266..6459468hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3826203
hg1926203
hg1826203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494233
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)nsv1044870
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