A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030445



Internal ID19119664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:254255..385056hg38UCSC Ensembl
Innerchr6:254255..385056hg19UCSC Ensembl
Innerchr6:199255..330056hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38130802
hg19130802
hg18130802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5878n100
Supporting Variantsnssv3650453
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)nsv1030445
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