A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042268



Internal ID19131487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55943048..56000537hg38UCSC Ensembl
Innerchr10:57702808..57760297hg19UCSC Ensembl
Innerchr10:57372814..57430303hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3857490
hg1957490
hg1857490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv868n100
Supporting Variantsnssv3506535
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)nsv1042268
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