A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037291



Internal ID19126510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70352092..70384654hg38UCSC Ensembl
Innerchr10:72111848..72144410hg19UCSC Ensembl
Innerchr10:71781854..71814416hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3832563
hg1932563
hg1832563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv922n100
Supporting Variantsnssv3504873
Samples
Known GenesLRRC20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037291
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