A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041174



Internal ID19130393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121004150..121030305hg38UCSC Ensembl
Innerchr10:122763663..122789818hg19UCSC Ensembl
Innerchr10:122753653..122779808hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3826156
hg1926156
hg1826156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv979n100
Supporting Variantsnssv3510943
Samples
Known GenesMIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041174
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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