A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037682



Internal ID18780213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..157806hg38UCSC Ensembl
Innerchr10:72797..203746hg19UCSC Ensembl
Innerchr10:62797..193746hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38130946
hg19130950
hg18130950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv648n100
Supporting Variantsnssv3484866
Samples
Known GenesTUBB8, ZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037682
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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