A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035118



Internal ID19124337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:258253..379003hg38UCSC Ensembl
Innerchr6:258253..379003hg19UCSC Ensembl
Innerchr6:203253..324003hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38120751
hg19120751
hg18120751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3652717, nssv3652716, nssv3652718
Samples
Known GenesDUSP22
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035118
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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