A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042172



Internal ID18784703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31324455..31384922hg38UCSC Ensembl
Innerchr10:31613384..31673851hg19UCSC Ensembl
Innerchr10:31653390..31713857hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3860468
hg1960468
hg1860468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv701n100
Supporting Variantsnssv3506443
Samples
Known GenesZEB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042172
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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