A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048131



Internal ID19137350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105560231..105745168hg38UCSC Ensembl
Innerchr10:107319989..107504926hg19UCSC Ensembl
Innerchr10:107309979..107494916hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38184938
hg19184938
hg18184938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510598
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)nsv1048131
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