A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045213



Internal ID19134432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121676951..121701392hg38UCSC Ensembl
Innerchr10:123436465..123460906hg19UCSC Ensembl
Innerchr10:123426455..123450896hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3824442
hg1924442
hg1824442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv985n100
Supporting Variantsnssv3514452, nssv3514592
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)nsv1045213
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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