A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047953



Internal ID19137172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128712001..128752732hg38UCSC Ensembl
Innerchr10:130510265..130550996hg19UCSC Ensembl
Innerchr10:130400255..130440986hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3840732
hg1940732
hg1840732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514479
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)nsv1047953
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